Liu, Yan team published research in Journal of Membrane Science in 2022 | 10111-08-7

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

Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. Their solubility in alcohol is lower than that in water and decreases with increasing molecular weight of the alcohols . Electric Literature of 10111-08-7.

Liu, Yan;Xie, Wei;Liang, Shuang;Li, Xingxun;Fan, Yanfang;Luo, Shuangjiang research published 《 Polyimide/ZIFs mixed matrix membranes with tunable interfacial interaction for efficient gas separation》, the research content is summarized as follows. Manipulating favorable interfacial microstructure is crucial to rationally design a high-performance mixed matrix membrane with defect-free interface. We describe herein an efficient pathway to finely tune the interfacial adhesion through balancing the metal organic frameworks and polymer functionality. The varied number of hydrogen bonds are established involving the CHO groups in hybrid ZIF-8-90(x) fillers with varied carboxaldehyde-2-imidazole linker contents and 6FDA-DAM:DABA copolyimides having adjustable COOH groups concentrations, thereby precisely controlling the membrane interfacial bonding behavior. As expected, the gas selectivity of the resulting membranes is gradually enhanced with increasing carboxaldehyde-2-imidazole linker substitution ratio in ZIF-8-90(x), mainly contributed by significant improvements in hydrogen bonding strength. The enhanced interaction is confirmed by good adhesion visualized in SEM images and the C=O vibration band shift in FTIR spectra. Meanwhile, adjusting the proportion of DABA moiety in polymers is an auxiliary path to regulate the interfacial bonding strength. The optimized membrane of 6FDA-DAM:DABA (1:1)/10 weight% ZIF-8-90(30) has enhanced H2/CH4 and CO2/CH4 ideal selectivities of 75.4 and 43.6, resp., with H2 and CO2 permeabilities of 222 Barrer and 128 Barrer. These findings imply that progressively regulating filler and polyimide functionality is a feasible route to finely tailor interfacial hydrogen bonding strength to achieve a membrane with tunable separation performance.

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