You, Bo team published research in ACS Earth and Space Chemistry in 2020 | 10111-08-7

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.

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