Synthesis and proton NMR spectra of 2-heteroaryl-substituted imidazo[4,5-b]pyridines and imidazo[4,5-c]pyridines was written by Yutilov, Yu. M.;Shcherbina, L. I.;Efremenko, A. F.. And the article was included in Khimiya Geterotsiklicheskikh Soedinenii in 1989.HPLC of Formula: 52538-09-7 The following contents are mentioned in the article:
The title compounds were prepared by oxidation of mixtures of 2,3- or 3,4-pyridinediamines with heterocycles containing an active Me group in the presence of S. Other methods involved cyclization of pyridinediamines with picoline N-oxides and 2-pyridinethiocarboxanilides and the intramol. oxidative cyclization of N4-(2-pyridylmethyl)-3,4-pyridinediamine. In most cases, the yield was â?0%. The NMR spectra of 2-pyridylimidazopyridines were examined This study involved multiple reactions and reactants, such as 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7HPLC of Formula: 52538-09-7).
2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.HPLC of Formula: 52538-09-7
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem