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. Recommanded Product: 1H-Imidazole-2-carbaldehyde.
Zhang, Xiao-Min;Yin, Jiao;Gao, Hong-Ling;Cui, Jian-Zhong research published 《 Five new multinuclear rare earth complexes: Magnetism and near-infrared luminescence》, the research content is summarized as follows. Five new tri- and tetra-nuclear rare earth complexes utilizing a Schiff base ligand and co-ligand Hdbm were obtained: [Nd3(dbm)6(H2L)3]·3CH3OH (1), [RE4(dbm)6(L)2(CH3OH)3]·2CH3OH (RE = Dy (2), Ho (3), Er (4), Yb (5)), (H3L = N’-(2-carboxide-imidazole)-[(2-hydroxy-3-methoxyphenyl)methylene]hydrazide, Hdbm = 1,3-diphenyl-1,3-propanedione). Complexes 2–5 are centrosym. tetranuclear complexes with eight-coordinated REIII ions, while complex 1 is a non-centrosym. trinuclear complex with nine-coordinated NdIII ions, which could be caused by lanthanide contraction. The magnetic properties studies show that 2 exhibits representative single-mol. magnets behavior, leading to an energy barrier of 25.3 K as well as pre-exponential factor of 7.21 × 10-7 s. Research on near-IR luminescence reveals that complexes 1, 3, 4 and 5 emit the characteristic emission peaks of the NdIII ions, HoIII ions, ErIII ions and YbIII ions, resp. The luminescence lifetime and quantum yield of 5 are 1.39μs and 0.0695%, resp.
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