110316-58-0

Basic information

• Product Name: (3R,4R,5R,6S)-4,5,6-Tris-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-1-((2R,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-heptan-3-ol
• Synonyms: (3R,4R,5R,6S)-4,5,6-Tris-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-1-((2R,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-heptan-3-ol
• CAS NO: 110316-58-0
• Molecular Weight: 1087.48
• Mol File: 110316-58-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3R,4R,5R,6S)-4,5,6-Tris-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-1-((2R,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-heptan-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,4R,5R,6S)-4,5,6-Tris-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-1-((2R,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-heptan-3-ol(110316-58-0)
• EPA Substance Registry System: (3R,4R,5R,6S)-4,5,6-Tris-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-1-((2R,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-heptan-3-ol(110316-58-0)

Safety Data

• Hazardous Substances Data: 110316-58-0(Hazardous Substances Data)

Upstream product

• 54423-54-0 2,3,4,6-Tetra-O-benzyl 1-O-p-nitrobenzoyl D-glucopyranoside 
• 110316-55-7 (2R,3R,4R,5S,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((Z)-2-iodo-vinyl)-tetrahydro-pyran 
• 110316-57-9 (Z)-(3R,4R,5R,6S)-4,5,6-Tris-benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-1-((2R,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-hept-1-en-3-ol 

Downstream Products

• 139195-36-1 (2S,3R,4R,5R)-2,3,4-Tris-benzyloxy-5-(tetrahydro-pyran-2-yloxy)-7-((2R,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-heptan-1-ol 
• 139195-38-3 C₆₃H₆₈O₁₀ 

Relevant articles and documents

Preferred Conformation of C-Glycosides. 2. Preferred Conformation of Carbon Analogues of Isomaltose and Gentiobiose

The preferred conformation of the methyl C-glycosides 1 and 2, carbon, analogues of methyl isomaltoside and methyl gentiobioside, was shown to be 1A and 2A, respectively, by 1H NMR spectroscopy.