774516-14-2

Basic information

• Product Name: (3aS,4R,5R,6S,6aS)-4-benzyloxy-6-benzyloxymethyl-2-dimethylamino-3a,5,6,6a-tetrahydro-4H-cyclopentimidazole-5-yl acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside
• Synonyms: (3aS,4R,5R,6S,6aS)-4-benzyloxy-6-benzyloxymethyl-2-dimethylamino-3a,5,6,6a-tetrahydro-4H-cyclopentimidazole-5-yl acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside
• CAS NO: 774516-14-2
• Molecular Weight: 869.07
• Mol File: 774516-14-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3aS,4R,5R,6S,6aS)-4-benzyloxy-6-benzyloxymethyl-2-dimethylamino-3a,5,6,6a-tetrahydro-4H-cyclopentimidazole-5-yl acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: (3aS,4R,5R,6S,6aS)-4-benzyloxy-6-benzyloxymethyl-2-dimethylamino-3a,5,6,6a-tetrahydro-4H-cyclopentimidazole-5-yl acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside(774516-14-2)
• EPA Substance Registry System: (3aS,4R,5R,6S,6aS)-4-benzyloxy-6-benzyloxymethyl-2-dimethylamino-3a,5,6,6a-tetrahydro-4H-cyclopentimidazole-5-yl acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside(774516-14-2)

Safety Data

• Hazardous Substances Data: 774516-14-2(Hazardous Substances Data)

Upstream product

• 175289-16-4 (1R,2R,3S,4S,5S)-3-acetamido-2-benzyloxy-4-(benzyloxy)amino-5-[(benzyloxy)methyl]cyclopentyl 2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 175289-17-5 (1R,2R,3S,4S,5S)-3-acetamido-2-benzyloxy-4-(N-benzyloxy-N-phenoxythiocarbonyl)amino-5-[(benzyloxy)methyl]cyclopentyl 2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 10511-03-2 dimethylammonium acetate 
• 175289-18-6 (3aS,4R,5R,6S,6aS)-6-benzyloxymethyl-1,4-dibenzyloxy-2-thio-2,3,3a,5,6,6a-hexahydro-4H-cyclopentimidazole-5-yl acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

Synthesis of a novel azapseudodisaccharide related to allosamidin employing N,N'-diacetylchitobiose as a key starting material

Design and synthesis of a potential chitinase inhibitor 4, related to allosamidin (2), is described. Radical cyclization mediated by tributyltin hydride was applied for the first time to chitobiose-derived oxime ethers 9a,b to give four stereoisomers of an aminocyclopentane derivative connected to an N-acetyl-D- glucosamine residue at C-1 position. The major isomer 10b was efficiently converted into a novel pseudodisaccharide 4 via a series of cyclic-guanidine formation reaction.