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

COA of Formula: C4H4N2O, 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 five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 10111-08-7, formula is C4H4N2O, Name is 1H-Imidazole-2-carbaldehyde. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. COA of Formula: C4H4N2O.

Woods, Ephraim;Harris, Oliver T.;Leiter, William E.;Burner, Nora E.;Ofosuhene, Pomaa;Krez, Alexandra;Hilton, Mark A.;Burke, Kathleen A. research published 《 Lifetime of Triplet Photosensitizers in Aerosol Using Time-Resolved Photoelectric Activity》, the research content is summarized as follows. Time-resolved photoelec. activity of aerosol (TPEAA) experiments measure the kinetics of photochem. initiated reactions near the surface of aerosol particles. In the demonstration presented here, TPEAA experiments monitor the evolution of excited triplet states, which are key intermediates in the photochem. formation of secondary organic aerosol (SOA). One example is the decay of the triplet excited state of imidazole-2-carboxaldehyde (IC) in aqueous NaCl aerosol particles. The decay of the triplet IC shows two distinct timescales, indicative of two populations of IC in the particles: aqueous and pure IC. The lifetime in the pure-IC phase is less than 20 ns, and the lifetime associated with aqueous IC is limited by reaction with chloride ions (k = 5.6 x 105 M-1 s-1). The results demonstrate how phase separation in aerosol particles can control reaction pathways and kinetics. In another example, TPEAA monitors the decay of the triplet anthraquinone-2-sulfonate (AQ2S) anion in aqueous NaCl aerosol. The AQ2S triplet reacts with water (k’ = 8.7 x 106 s-1) to produce adduct species. In this case, tuning the wavelength of the photoemission laser permits the preferential observation of the triplet or a combination of the AQ2S triplet and the water adduct. These results bridge a gap between aerosol phase measurements, which are normally steady-state and bulk-phase transient absorption measurements, which typically probe homogeneous phases.

COA of Formula: C4H4N2O, 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