244037-03-4

Basic information

• Product Name: (5R,6R,7S,8R)-7,8-bis(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydro-2-iodo-6-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)imidazo[1,2-a]pyridine
• Synonyms: (5R,6R,7S,8R)-7,8-bis(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydro-2-iodo-6-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)imidazo[1,2-a]pyridine
• CAS NO: 244037-03-4
• Molecular Weight: 1119.11
• Mol File: 244037-03-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (5R,6R,7S,8R)-7,8-bis(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydro-2-iodo-6-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)imidazo[1,2-a]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: (5R,6R,7S,8R)-7,8-bis(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydro-2-iodo-6-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)imidazo[1,2-a]pyridine(244037-03-4)
• EPA Substance Registry System: (5R,6R,7S,8R)-7,8-bis(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydro-2-iodo-6-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)imidazo[1,2-a]pyridine(244037-03-4)

Safety Data

• Hazardous Substances Data: 244037-03-4(Hazardous Substances Data)

Upstream product

• 244036-92-8 2,3,6-tri-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-D-gluconamide 
• 244036-97-3 5-amino-2,3,6-tri-O-benzyl-5-deoxy-4-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-1-thio-D-gluconolactam 
• 221681-65-8 5-amino-2,3,6-tri-O-benzyl-5-deoxy-4-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-L-glucono-1,5-lactam 
• 88970-25-6 2,3,6-tri-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-D-glucono-1,5-lactone 
• 148968-90-5 2,3,6-tris-O-(phenylmethyl)-4-O-[2,3,4,6-tetrakis-O-(phenylmethyl)-β-D-glucopyranosyl]-D-glucopyranoside 
• 244037-01-2 (5R,6R,7S,8R)-7,8-bis(benzyloxy)-5-[(benzyloxy)methyl]-5,6,7,8-tetrahydro-2,3-diiodo-6-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)imidazo[1,2-a]pyridine 

Relevant articles and documents

Inhibition of cellobiohydrolases from Trichoderma reesei. Synthesis and evaluation of some glucose-, cellobiose-, and cellotriose-derived hydroximolactams and imidazoles

The lactam 16, the hydroximolactams 8, 20, 23, and 27, and the imidazole 32 were prepared following known methods. They were tested together with the known tetrazole 35 and the hydroximolactams 2 and 36 as inhibitors of the cellobiohydrolases Ce17A and Ce