860634-49-7

Basic information

• Product Name: 1,6-anhydro-3-{(1R)-2,6-anhydro-3,4,5,7-tetra-O-[(tert-butyl)dimethylsilyl]-D-glycero-L-manno-heptitol-1-C-yl}-2-[(N-benzyl-N-methoxy)amino]-2,3-dideoxy-β-D-galacto-hexopyranose
• Synonyms: 1,6-anhydro-3-{(1R)-2,6-anhydro-3,4,5,7-tetra-O-[(tert-butyl)dimethylsilyl]-D-glycero-L-manno-heptitol-1-C-yl}-2-[(N-benzyl-N-methoxy)amino]-2,3-dideoxy-β-D-galacto-hexopyranose
• CAS NO: 860634-49-7
• Molecular Weight: 914.528
• Mol File: 860634-49-7.mol

Chemical Properties

• CAS DataBase Reference: 1,6-anhydro-3-{(1R)-2,6-anhydro-3,4,5,7-tetra-O-[(tert-butyl)dimethylsilyl]-D-glycero-L-manno-heptitol-1-C-yl}-2-[(N-benzyl-N-methoxy)amino]-2,3-dideoxy-β-D-galacto-hexopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-anhydro-3-{(1R)-2,6-anhydro-3,4,5,7-tetra-O-[(tert-butyl)dimethylsilyl]-D-glycero-L-manno-heptitol-1-C-yl}-2-[(N-benzyl-N-methoxy)amino]-2,3-dideoxy-β-D-galacto-hexopyranose(860634-49-7)
• EPA Substance Registry System: 1,6-anhydro-3-{(1R)-2,6-anhydro-3,4,5,7-tetra-O-[(tert-butyl)dimethylsilyl]-D-glycero-L-manno-heptitol-1-C-yl}-2-[(N-benzyl-N-methoxy)amino]-2,3-dideoxy-β-D-galacto-hexopyranose(860634-49-7)

Safety Data

• Hazardous Substances Data: 860634-49-7(Hazardous Substances Data)

Upstream product

• 328386-10-3 1,6-Anhydro-3-C-{(1R)-2,6-anhydro-3,4,5,7-tetra-O-[(tert-butyl)dimethylsilyl]-D-glycero-L-manno-heptitol-1-C-yl}-2,3-dideoxy-β-D-glycero-hex-2-enopyranos-4-ulose 
• 328386-07-8 2,3,4,6-Tetra-O-[(tert-butyl)dimethylsilyl]-C-β-D-galactopyranosylformaldehyde 
• 33647-85-7 isolevoglucosenone 
• 860634-47-5 1,6-anhydro-3-{(1R)-2,6-anhydro-3,4,5,7-tetrakis-O-[(tert-butyl)dimethylsilyl]-D-glycero-L-manno-heptitol-1-C-yl}-2-[(N-benzyl-N-methoxy)amino]-2,3-dideoxy-β-D-xylo-hexopyran-4-ulose 

Relevant articles and documents

C-linked disaccharide analogue of the Thomsen-Friedenreich (T)-epitope α-O-conjugated to L-serine

Condensation of a silylated β-D-galactopyranosylaldehyde (3) with isolevoglucosenone (4) in the presence of Et2AlI provided bicyclic enone 5. Subsequent addition of BnNHOMe gave adduct 6, which was converted into 4-O-acetyl-1,6-anhydro-3-C-[(1R