Tag: M.W=50-100

Imidazole based anticancer drug find applications in cancer chemotherapy. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). Electric Literature of 10111-08-7.

Xu, Yu;Zhang, Xiu-Juan;Li, Wen-Bo;Wang, Xing-Rong;Wang, Shuai;Qiao, Xue-Peng;Chen, Shi-Wu research published 《 Design, synthesis and biological evaluation of indole-2-one derivatives as potent BRD4 inhibitors》, the research content is summarized as follows. A series of indole-2-one derivatives I (R¹ = cyclopropyl, cyclopentyl, 4,5-dihydro-1H-imidazol-2-yl, etc.; R² = H, Me, cyclopropyl, furan-2-yl; R³ = 4-methoxyphenyl, 2,5-difluorophenyl, naphthalen-1-yl, etc.; R¹R² = -(CH₂)₃-, -(CH₂)₅-) and II (R⁴ = 2-methoxyphenyl, cyclohexyl) through scaffold hopping drug design has been designed and synthesized. Most of the compounds showed potent BRD4 inhibitory activities and anti-proliferation activities in cancer cell lines. Especially, compound I (R¹ R² = -(CH₂)₃-; R³ = 2-methoxyphenyl) (II) exhibited excellent BRD4 inhibitory activities (BD1 IC₅₀ = 19 nM, BD2 IC₅₀ = 28 nM) and anti-proliferation potency with IC₅₀ values of 4.75μM and 1.35μM in HT-29 and HL-60 cells, resp. Addnl., docking studies showed that the hydrophobic pocket next to KAc region and WPF shelf were critical to the activity of the compound Compound II could arrest the cell-cycle progression of HT-29 cells into the G1 phase and reduce the expression of c-Myc. Moreover, compound II exhibited favorable oral pharmacokinetic properties. All the results demonstrated that compound II was a potent BRD4 inhibitor and had merely potential for colon cancer treatment.

10111-08-7, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., Electric Literature of 10111-08-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Category: imidazoles-derivatives.

Xue, Lei;Zhang, Aiai;Wu, Jinfang;Wang, Qi;Liu, Yang;Zhao, Yuansong;Liu, Shangpeng;Liu, Ze;Li, Ping;Zeng, Shanghong research published 《 Surface modification and reconstruction of ZnO hollow microspheres for selective electroreduction of CO₂ to CO》, the research content is summarized as follows. Surface chem. can be modified by introducing another component on the surface of catalyst due to the regulation of configuration and electronic properties. Herein, the nanostructured ZnO hollow microspheres were fabricated for selective CO₂ reduction to CO. The addition of CuO weakens the strength of adjacent Zn-O bond and improves the formation of more zero-valence Zn. Small CuO entities can provide the active sites for CO₂ adsorption, and the presence of surface defects due to Zn²⁺ reduction could enhance initial dissociation from CO₂ to CO. More interestingly, the 3CuO/ZnO catalyst underwent reconstruction during electrocatalysis, and multi-shelled hollow spheres evolved into a thin flaky structure. The extended surface area of flaky morphol. enhances the catalytic stability despite the occurrence of ZnO reduction This study highlights the importance of surface modification for CO₂ selective reduction to CO but also provides some insights on reconstruction during electrochem. reduction of CO₂.

Category: imidazoles-derivatives, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., 10111-08-7.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole Biochem/physiol Actions: Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. It also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes. Recommanded Product: 1H-Imidazole-2-carbaldehyde.

Yadav, Manoj Kumar;Pokhrel, Shanta;Yadav, Paras Nath research published 《 Novel chitosan derivatives of 2-imidazolecarboxaldehyde and 2-thiophenecarboxaldehyde and their antibacterial activity》, the research content is summarized as follows. Chitosan was synthesized from chitin; extracted from prawn shells’ powder via deacetylation and physicochem. properties were studied. Novel chitosan derivatives of 2-imidazolecarboxaldehyde and 2-thiophenecarboxaldehyde were synthesized by refluxing equimolar quantities of resp. aldehyde with chitosan. These functionalized chitosan derivatives were characterized by Fourier transform IR (FTIR), ¹³C-NMR (¹³C-NMR) spectroscopy, elemental anal., X-ray diffraction (XRD), thermogravimetric anal. (TGA) and DTA (DTA) and their antibacterial activity was explored. Chitosan derivative of 2-thiophenecarboxaldehyde was found active against Escherichia coli.

Recommanded Product: 1H-Imidazole-2-carbaldehyde, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., 10111-08-7.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Application of C5H8N2.

Yan, Wenjun;Xu, Huoshu;Ling, Min;Zhou, Shiyu;Qiu, Tong;Deng, Yanjun;Zhao, Zhidong;Zhang, Erpan research published 《 MOF-Derived Porous Hollow Co₃O₄@ZnO Cages for High-Performance MEMS Trimethylamine Sensors》, the research content is summarized as follows. Trimethylamine (TMA) sensors based on metal oxide semiconductors (MOS) have drawn great attention for real-time seafood quality evaluation. However, poor selectivity and baseline drift limit the practical applications of MOS TMA sensors. Engineering core@shell heterojunction structures with accumulation and depletion layers formed at the interface is regarded as an appealing way for enhanced gas sensing performances. Herein, we design porous hollow Co₃O₄@ZnO cages via a facile ZIF-67@ZIF-8-derived approach for TMA sensors. These sensors demonstrate great TMA resistive sensing performance (linear response at moderate TMA concentrations (<33 ppm)), and a high sensitivity of ~41 is observed when exposed to 33 ppm TMA, with a response/recovery time of only 3/2 s. This superior performance benefits from the Co₃O₄@ZnO porous hollow structure with maximum heterojunctions and high surface area. Furthermore, great capacitive TMA sensing with linear sensitivity over the full testing concentration range (0.33-66 ppm) and better baseline stability were investigated. A possible capacitive sensing mechanism of TMA polarization was proposed. For practical usage, a portable sensing prototype based on the Co₃O₄@ZnO sensor was fabricated, and its satisfactory sensing behavior further confirms the potential for real-time TMA detection.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Application of C5H8N2

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole Biochem/physiol Actions: Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. It also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes. Formula: C4H4N2O.

Yang, Yi;Csakai, Adam;Jiang, Shuangshuang;Smith, Christina;Tanji, Hiromi;Huang, Jian;Jones, Torey;Sakaniwa, Kentaro;Broadwell, Lindsey;Shi, Chengrui;Soti, Subada;Ohto, Umeharu;Fang, Yaohui;Shen, Shu;Deng, Fei;Shimizu, Toshiyuki;Yin, Hang research published 《 Tetrasubstituted imidazoles as incognito Toll-like receptor 8 a(nta)gonists》, the research content is summarized as follows. Small-mol. modulators of TLR8 have drawn much interests as it plays pivotal roles in the innate immune response to single-stranded RNAs (ssRNAs) derived from viruses. However, their clin. uses are limited because they can invoke an uncontrolled, global inflammatory response. The efforts described herein culminate in the fortuitous discovery of a tetrasubstituted imidazole CU-CPD107 which inhibits R848-induced TLR8 signaling. In stark contrast, CU-CPD107 shows unexpected synergistic agonist activities in the presence of ssRNA, while CU-CPD107 alone is unable to influence TLR8 signaling. CU-CPD107′s unique, dichotomous behavior sheds light on a way to approach TLR agonists. CU-CPD107 offers the opportunity to avoid the undesired, global inflammation side effects that have rendered imidazoquinolines clin. irrelevant, providing an insight for the development of antiviral drugs.

Formula: C4H4N2O, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., 10111-08-7.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole based anticancer drug find applications in cancer chemotherapy. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). SDS of cas: 1739-84-0.

Yao, Shan-Shan;Wang, Hong;Jin, Fan-Long;Park, Soo-Jin research published 《 Synthesis of the ionic liquid 1,2-dimethyl-3-butylimidazole bromide salt and its application in phenolic-formaldehyde-resin-based conductive materials》, the research content is summarized as follows. Herein, the ionic liquid 1,2-dimethyl-3-butylimidazole bromide salt ([DMBIm]Br) was synthesized and its chem. structure was characterized via Fourier transform IR and ¹H NMR spectroscopies. Moreover, to improve the elec. property of the phenolic formaldehyde (PF) resin, PF/[DMBIm]Br systems were prepared via a melt blending and compression-curing process. Furthermore, the effect of [DMBIm]Br content on the thermal stabilities, mech. properties, elec. properties, and morphologies of the systems was investigated. The thermal stability of the systems increased with [DMBIm]Br addition The impact strength of the systems improved with increasing [DMBIm]Br content. Addnl., the volume resistance of the systems significantly decreased from 1.02 x 10⁹ to 1.64 x 10⁷ Ω with increasing [DMBIm]Br content from 0 to 1 wt%.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., SDS of cas: 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Application In Synthesis of 1739-84-0.

Yin, Wenyan;Zhang, Milin;Liu, Jingyuan;Alali, Khaled Tawfik;Yu, Jing;Zhu, Jiahui;Liu, Peili;Li, Rumin;Wang, Jun research published 《 MOF-derived electrochemical catalyst Cu-N/C for the enhancement of amperometric oxygen detection》, the research content is summarized as follows. Electrochem. sensors using ionic liquids as electrolytes for oxygen detection are now getting more and more attention. Recently, an ionic liquid combined with an electrochem. active catalyst system has become popular for boosting the sensing performance of oxygen sensors. In this work, the imidazolyl-based ionic liquid 1-butyl-2,3-dimethylimidazole bis((trifluoromethyl)sulfonyl)imide [Bmmim][TFSI] is first prepared by a facile two-step method. Subsequently, a transition metal and N-codoped porous carbon oxygen reduction electrochem. catalyst Cu-N/C is synthesized by calcining the Cu-doped ZIF-8 precursor and then blending it in different ratios with the ionic liquid [Bmmim][TFSI] as composite electrolytes for oxygen detection. The composite electrolyte Cu-N/C/[Bmmim][TFSI] exhibits increased responses in cyclic voltammetry (CV) and chronoamperometry (CA) relative to that of the pure ionic liquid Furthermore, the CV and CA data show that 6% Cu-N/C/[Bmmim][TFSI] has the optimum oxygen sensing response with an enhanced reduction peak current, a sensitivity of 0.1678 μA/[% O₂] and a good linear fitting coefficient of 0.9991. In conclusion, the results confirm the success of using Cu-N/C as an electrochem. catalyst composed of the Cu-N/C/[Bmmim][TFSI] electrolyte for improving the responsivity, stability and sensitivity towards a wide range of oxygen concentrations

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Application In Synthesis of 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole based anticancer drug find applications in cancer chemotherapy. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). Safety of 1H-Imidazole-2-carbaldehyde.

Yoo, Miri;Koh, Dongsoo research published 《 Diethyl 4-(1H-imidazol-2-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate》, the research content is summarized as follows. In the title compound, C₁₆H₂₁N₃O₄, the 1,4-dihydropyridine ring adopts a flattened boat conformation, with the imidazole substituent in an axial orientation [dihedral angle between ring planes = 82.9 (6)°]. In the crystal structure, pairs of N-H···O and N-H···N hydrogen bonds with graph-set notation R²₂(14) connect the mols. into chains running along the c-axis direction.

10111-08-7, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., Safety of 1H-Imidazole-2-carbaldehyde

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Computed Properties of 10111-08-7.

Yoshida, Shuhei;Uehara, Shota;Kondo, Noriyasu;Takahashi, Yu;Yamamoto, Shiho;Kameda, Atsushi;Kawagoe, Soichiro;Inoue, Naoko;Yamada, Masami;Yoshimura, Norito;Tachibana, Yuki research published 《 Peptide-to-Small Molecule: A Pharmacophore-Guided Small Molecule Lead Generation Strategy from High-Affinity Macrocyclic Peptides》, the research content is summarized as follows. Recent technol. innovations have led to the development of methods for the rapid identification of high-affinity macrocyclic peptides for a wide range of targets; however, it is still challenging to achieve the desired activity and membrane permeability at the same time. Here, we propose a novel small mol. lead discovery strategy, ′′Peptide-to-Small Mol.′′, which is a combination of rapid identification of high-affinity macrocyclic peptides via peptide display screening followed by pharmacophore-guided de novo design of small mols., and demonstrate the applicability using nicotinamide N-methyltransferase (NNMT) as a target. Affinity selection by peptide display technol. identified macrocyclic peptide 1 that exhibited good enzymic inhibitory activity but no cell-based activity. Thereafter, a peptide pharmacophore-guided de novo design and further structure-based optimization resulted in highly potent and cell-active small mol. 14 (cell-free IC₅₀ = 0.0011 μM, cell-based IC₅₀ = 0.40 μM), indicating that this strategy could be a new option for drug discovery.

Computed Properties of 10111-08-7, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., 10111-08-7.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents. Related Products of 10111-08-7.

You, Bo;Li, Siyang;Tsona, Narcisse T.;Li, Jianlong;Xu, Li;Yang, Zhaomin;Cheng, Shumin;Chen, Qingcai;George, Christian;Ge, Maofa;Du, Lin research published 《 Environmental Processing of Short-Chain Fatty Alcohols Induced by Photosensitized Chemistry of Brown Carbons》, the research content is summarized as follows. Fatty alcs. are known surfactants ubiquitous in the environment. They affect physicochem. and optical properties of aerosols and air/water interfaces; however, little is known about their photochem. Brown carbon (BrC) as photosensitizer, may initiate photochem. reactions of such non-photoactive surfactants. BrC was obtained by evaporating methylglyoxal/(NH₄)₂SO₄ or methylglyoxal/glycine (Gly) mixtures The BrC photo-sensitization ability was evidenced by its reaction with 1-octanol under UV irradiation measured by attenuated total reflection Fourier transform IR spectrometry, a surface-sensitive technique. Condensed phase products were determined by gas chromatog./mass spectrometry. A series of functionalized, unsaturated compounds were formed by a photo-sensitized reaction; more highly oxygenated compounds appeared after a long illumination time. This process contributed to formation of reactive volatile and semi-volatile organic compounds and could also trigger secondary chem. The reaction was probably initiated by electronically excited BrC upon exposure to UV radiation. A possible mechanism for fatty alcs. photo-sensitized degradation is proposed. It was also observed that BrC was easily photo-bleached; thus, it has a limited effect on radiative forcing. However, BrC can play an important role in aerosol and air/water interfaces.

Related Products of 10111-08-7, 1H-Imidazole-2-carbaldehyde, also known as 1H-Imidazole-2-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
1H-Imidazole-2-carboxaldehyde is a novel PTP1b inhibitor with potential application to treat type 2 diabetes.
1H-Imidazole-2-carboxaldehyde is a broad-spectrum antimicrobial that has been shown to inhibit the growth of bacteria by interfering with protein synthesis. It binds to the cytosolic protein and receptor molecule, which are involved in the activation of bacterial enzymes. Imidazole-2-carboxaldehyde reacts with anhydrous sodium and copper complex to produce hydrogen bonds, which prevent the formation of the nitrogen atoms necessary for cellular processes. This chemical also has biological properties such as glyoxal, which inhibits bacterial growth by reacting with amino groups on proteins., 10111-08-7.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem