The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. 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. Safety of 1H-Imidazole-2-carbaldehyde.
Guo, Shen;Zhang, Shu-Hua;Wang, Fei;Zhang, Jian research published 《 Syntheses of tetrahedral imidazolate frameworks with auxiliary ligand in DMSO》, the research content is summarized as follows. In the authors’ former work, the authors developed one kind of new tetrahedral imidazolate frameworks (TIF-Ax) by adding auxiliary unineg. linker into the zinc-imidazolate assembly in amide. Herein, (TIF-A4 to TIF-A8) were obtained from imidazolate derivatives and Zinc acetate (acetate as auxiliary ligands) in DMSO. Among them, Zn centers were coordinated by imidazolate derivatives to form 1-dimensional chain, differently, TIF-A4 exhibited 3-dimensional framework with dia topol. and TIF-A5 to TIF-A8 were 4-connected layer with sql topol. These results suggested that DMSO was a good solvent for the syntheses of new TIF-Ax. These compounds were characterized by single crystal XRD, powder XRD, FTIR and TG. The fluorescence of them were also tested.
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