Category: 1374155-84-6

Crystal structure of poly[diaqua-bis(μ₂-thiophene-2,5-dicarboxylate-κ²O:O’)(3,5-di(1H-imidazol-1-yl)pyridine-κ²N:N’)cobalt(II)], Co(H₂O)₂(C₆H₂O₄S)(C₁₁N₄H₉), C₁₇H₁₅CoN₅O₆S was written by Liu, Shu-Hua;Xu, Qing-Zhong;Li, Sai-Yu;Zhang, Rui-Ling;Wang, Li-Hong;Liu, Jian-Hua. And the article was included in Zeitschrift fuer Kristallographie – New Crystal Structures in 2014.Recommanded Product: 3,5-Di(1H-imidazol-1-yl)pyridine The following contents are mentioned in the article:

This article discusses on crystal structure of poly[diaqua-bis(μ₂-thiophene-2,5-dicarboxylate-κ²O:O’)(3,5-di(1H-imidazol-1-yl)pyridine-κ²N:N’)cobalt(II)], Co(H₂O)₂(C₆H₂O₄S)(C₁₁N₄H₉),C₁₇H₁₅CoN₅O₆S. Thus on hydrothermal synthesis and crystal structure of a new cobalt coordination polymer based on the tdc^2- dianion and 3,5-di(1H-imidazol-1-yl)pyridine ligands is also discussed. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Recommanded Product: 3,5-Di(1H-imidazol-1-yl)pyridine).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Recommanded Product: 3,5-Di(1H-imidazol-1-yl)pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Hydrothermal synthesis, crystal structures, and photoluminescent properties of two cadmium(II) coordination polymers derived from dicarboxylates and N-donor ligands was written by Xu, Jiakun;Sun, Xiaochun;Ju, Caixia;Yang, Lirong;Bi, Caifeng;Sun, Mi. And the article was included in Journal of Coordination Chemistry in 2013.Product Details of 1374155-84-6 The following contents are mentioned in the article:

Two metal coordination polymers, [Cd(ipa)(L₁)(H₂O)]_n (1) and [Cd(ipa)(L₂)]_n (2) [H₂ipa = isophthalic acid, L₁ = 3,5-bis(imidazol-1-yl)pyridine and L₂ = 3,5-bis(benzoimidazol-1-yl)pyridine], were synthesized and structurally characterized by IR, elemental anal., XRD, and x-ray single-crystal diffraction. Complex 1 shows a 2-fold cds topol. net and 2 features a 3-dimensional pcu topol. net. Luminescent properties of 1 and 2 were studied in the solid state at room temperature This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Product Details of 1374155-84-6).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Product Details of 1374155-84-6

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Suzuki-Miyaura C-C coupling reactions catalysed by a homogeneous and nanosilica supported palladium(II) N-heterocyclic carbene complex derived from 3,5-di(1-imidazolyl)pyridine was written by Pahlevanneshan, Zari;Moghadam, Majid;Mirkhani, Valiollah;Tangestaninejad, Shahram;Mohammadpoor-Baltork, Iraj;Rezaei, Saghar. And the article was included in New Journal of Chemistry in 2015.Name: 3,5-Di(1H-imidazol-1-yl)pyridine The following contents are mentioned in the article:

A new Pd N-heterocyclic carbene complex using 3,5-di(1H-imidazol-1-yl)pyridine as a precursor was prepared The complex was immobilized on 3-chloropropylated nanosilica as a support and characterized by FTIR spectroscopy, TGA, field emission SEM, energy dispersive x-ray anal., TEM and elemental anal. The prepared catalyst was used as a heterogeneous catalyst in the Suzuki-Miyaura coupling reactions of various aryl halides with phenylboronic acid and the corresponding biphenyls were being produced in a high yield. The catalyst was recyclable under aerobic conditions without significant loss of activity. Also, the catalytic activity of the homogeneous catalyst was studied. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Name: 3,5-Di(1H-imidazol-1-yl)pyridine).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Name: 3,5-Di(1H-imidazol-1-yl)pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Improving effect of Co(II)-coordination polymers on pre-eclampsia symptoms by increasing the Elabela was written by Chen, Xue-Jun;Tao, Xiao-Ling;Li, Lan-Fang;Lu, Wen-Hao;Wang, Ya-Ping. And the article was included in Inorganic and Nano-Metal Chemistry in 2022.Name: 3,5-Di(1H-imidazol-1-yl)pyridine The following contents are mentioned in the article:

Two Co(II)-coordination polymers modified by a rigid amine 3,5-bis(imidazole-1-yl)pyridine (BIP), [Co₂(HPO₃)₂(BIP)]·H₂O () and [Co₃(HPO₃)₃(BIP)(H₂O)]·H₂O (), were solvothermally prepared Their improving effect on pre-eclampsia symptoms was evaluated and the related mechanism was explored at the same time. Firstly, the ELISA detection kits were performed to measure the levels of the Elabela in the plasma after indicated treatment. In addition to this, the urine protein content of pregnant mice after compound treatment was also determined with Braford protein content detection kit. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Name: 3,5-Di(1H-imidazol-1-yl)pyridine).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.Name: 3,5-Di(1H-imidazol-1-yl)pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

The Syntheses, Structures, Fluorescence Properties and Biological Activity of two Novel Zinc(II) Complexes Controlled by the Tripodal Imidazole Ligand was written by Gao, En-Jun;Zhang, Shaozhong;Meng, Yang;Zhao, Fu-Chen;Ma, Xiao-Yu;Jin, Hai-Tao;Liu, Si-Jia;Ge, Jing;Sun, Ya-Guang;Zhang, Wan-zhong;Zhu, Ming-Chang. And the article was included in Journal of Fluorescence in 2016.Product Details of 1374155-84-6 The following contents are mentioned in the article:

Two new zinc complexes, namely Zn(L¹)ClCH₂NO(1) and {Zn(L²)CH₂NO}_n N(CH₃)₃ ClO₄(2) (L¹ = 3,5-di(1H-imidazol-1-yl)pyridine L² = 1,3,5-tris(1-imidazolyl) benzene), have been synthesized, and characterized by IR spectra, elemental anal., and a single crystal X-ray diffraction. Fluorescence spectroscopy indicated that two complexes presented strong DNA binding affinity constants to fish sperm DNA (FS-DNA). Gel electrophoresis assay demonstrated the ability of the complex to cleave the HL-60 DNA. Apoptotic study showed the complex exhibited significant cancer cell(KB) inhibitory rate. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Product Details of 1374155-84-6).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. Imidazole is the basic core of some natural products such as histidine, purine, histamine and DNA based structures, etc. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.Product Details of 1374155-84-6

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Zinc coordination polymers with rigid dicarboxylates and semirigid 3,5-bis(imidazole-1-yl) pyridine: syntheses, structural topologies, and luminescent properties was written by Xu, Jiakun;Sun, Xiaochun;Ju, Caixia;Sheng, Jun;Wang, Fang;Sun, Mi. And the article was included in Journal of Coordination Chemistry in 2013.Formula: C11H9N5 The following contents are mentioned in the article:

Two metal coordination polymers, {[Zn(bpdc)(bip)]·2H₂O}_n (1) and [Zn(tdc)(bip)] (2) [H₂bpdc (5) = biphenyl-4,4′-dicarboxylate, H₂tdc (7) = thiophene-2,5-dicarboxylate, bip (6) = 3,5-bis(imidazole-1-yl)pyridine], were synthesized and characterized by IR, elemental anal., XRD, and x-ray single-crystal diffraction. In, bpdc and bip link Zn(II) ions into a corrugated 2D layer. The corrugated 2D layers polycatenate each other, yielding a 2Dâ†?D polycatenation net. In, dinuclear Zn(II) units are formed by bip and further connected by tdc to construct a 2D 3-connected framework. The luminescent properties of and were studied in the solid state at room temperature This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Formula: C11H9N5).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Formula: C11H9N5

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Two- and three-dimensional hybrid zinc phosphites: syntheses, structures and photoluminescence properties was written by Han, Song-De;Zhang, Xiu-Rong;Pan, Jie;Mu, Ying;Li, Jin-Hua;Wang, Guo-Ming. And the article was included in Dalton Transactions in 2018.Synthetic Route of C11H9N5 The following contents are mentioned in the article:

Two zinc-phosphites modified by a rigid amine 3,5-bis(imidazole-1-yl)pyridine (BIP), [Zn₂(HPO₃)₂(BIP)]·H₂O (1) and [Zn₃(HPO₃)₃(BIP)(H₂O)]·H₂O (2), were solvothermally prepared Compound 1 possesses a zincophosphite layer decorated by BIP moieties via coordinating to intralayer Zn(II) ions. Compound 2 features a 3-dimensional frame with a pillar-layer structure, in which the organic BIP pillars the inorganic zincophosphite layer via coordinating to interlayer Zn(II) ions. The structural diversity from a 2-dimensional layer to a 3-dimensional frame was mainly attributable to the different bridging modes of BIP in the process of assembly. Their temperature-dependent photoluminescence properties also were studied. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Synthetic Route of C11H9N5).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Synthetic Route of C11H9N5

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Two novel Co (II) bifunctional MOFs: Syntheses and applications in photocatalytic degradation of dyes and electrocatalytic water oxidation was written by Cui, Guanning;Liu, Wenbo;Wang, Lulu;Wu, Ruixue;Bi, Caifeng;Zhang, Dongmei;Fan, Yuhua. And the article was included in Journal of Solid State Chemistry in 2021.Safety of 3,5-Di(1H-imidazol-1-yl)pyridine The following contents are mentioned in the article:

Two novel Co (II) MOFs based on 5-(4-(imidazolyl-1-yl)phenyl) isophthalic acid (H₂L), [Co(L)(tib)(H₂O)₂]_n (CP 1) and [Co(L)(bip)_0.5]_n (CP 2) (tib = 1,3,5-tris (1-imidazolyl) benzene, bip = 3,5-bis(1-imidazolyl) pyridine ether) were synthesized under solvothermal conditions and characterized by powder x-ray diffraction, single crystal x-ray diffraction. The photodegradation studies demonstrate that CPs 1–2 show high-efficiency degradation of MV (Methyl violet), and the mechanism studies demonstrate that the main active species are ·OH radicals. Meanwhile, electrochem. studies demonstrate that CPs 1–2 can catalyze water oxidation under alk. conditions, and CPs 1–2 only need the overpotential of 348 mV-760 mV to deliver the c.d. of 1 mA cm^-2. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Safety of 3,5-Di(1H-imidazol-1-yl)pyridine).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.Safety of 3,5-Di(1H-imidazol-1-yl)pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Two dimensional coordination polymers based on 3,5-di(1H-imidazol-1-yl)pyridine and their fluorescence properties was written by Zhang, Hao;Zhu, Zhao Qiang;Zhou, Fu-Hou;Redshaw, Carl;Chen, Kai;Xu, Jing. And the article was included in Journal of Molecular Structure in 2020.Application In Synthesis of 3,5-Di(1H-imidazol-1-yl)pyridine The following contents are mentioned in the article:

The solvothermal synthesis of three new 2D MOFs is reported. From the reaction of 3,5-di(1H-imidazol-1-yl)pyridine (dip) and the metal salts Co(NO₃)₂·6H₂O, Cd(NO₃)₂·4H₂O or Zn(NO₃)₂·4H₂O, the three MOFs [Co(dip)₂(SCN)₂] (1), {[Cd(dip)₂(H₂O)₂]·(NO₃)₂} (2), {[Zn(dip)₂(H₂O)₂]·(ClO₄)₂} (3) were obtained. For these 2D MOFs, all the metal ions adopt a six-coordinate octahedral geometry with axial coordination sites occupied by SCN^– or water mols. The SCN^–/water ligands were all mono-coordinate and led to layered MOF structures. Furthermore, the fluorescence properties of 2 and 3 have been investigated. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Application In Synthesis of 3,5-Di(1H-imidazol-1-yl)pyridine).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Application In Synthesis of 3,5-Di(1H-imidazol-1-yl)pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

The preventive effect of two coordination polymers in the treatment of hypotension after uterine oviduct and ovarian surgery was written by Li, Chang-Kun;Ren, Xiao-Jing;Zhang, Jing-Yi;Zheng, Zhong-Lei;Du, Ke-Xin. And the article was included in Latin American Journal of Pharmacy in 2022.Synthetic Route of C11H9N5 The following contents are mentioned in the article:

In the current study, via using the mixed-ligand synthesis approach, two new Cu(II) and Co(II)-containing coordination polymers (CPs) with the chem. compositions of {[Cu2(L)[H(1,4-bmib)]]·1.5(H2O)}n (11, 1,4-bmib = 1,4-bis(2-methylimidazol-1-yl)butane) and {[Co2(HL)(3,5-bip)2]·(H2O)}n (2, 3,5-bip = 3,5-bis(1-imidazolyl) pyridine) have been successfully prepared by reaction of the corresponding metal salts with the flexible carboxylic ligand 3,5-bis(3,5-dicarboxylphenoxy)benzoic acid (H5L) in the presence of different N-donor co-ligands. Furthermore, the biol. activity of compounds 1 and 25 on the hypotension after uterine oviduct and ovarian surgery was evaluated and the related mechanism was explored at the same time. Firstly, the blood pressure of the hypotension animal model was measured. Besides, the relative expression of the α receptors on peripheral small blood vessels was determined with real time RT-PCR assay. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Synthetic Route of C11H9N5).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Synthetic Route of C11H9N5

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem