Determination of the structure of 2-methylimidazo[4,5-c]pyridine glycosides was written by Miroshnichenko, N. S.;Kovalenko, A. S.;Stetsenko, A. V.. And the article was included in Ukrainskii Khimicheskii Zhurnal (Russian Edition) in 1974.Related Products of 52538-09-7 The following contents are mentioned in the article:
Imidazopyridine glycosides (I; R = tri-O-acetyl-β-D-ribopyranosyl, β-D-ribopyranosyl, tri-O-acetyl-β-D-xylopyranosyl β-D-xylopyranosyl, tetra-O-acetyl-β-D-galactopyranosyl, β-D-galactopyranosyl) were prepared by known methods in 49-86%yields and their structures confirmed by NMR. This study involved multiple reactions and reactants, such as 2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7Related Products of 52538-09-7).
2,3-Dimethyl-3H-imidazo[4,5-c]pyridine (cas: 52538-09-7) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Related Products of 52538-09-7
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem