79258-16-5

Basic information

• Product Name: 2,6-anhydro-1,3,4,5-tetra-O-benzyl-D-glycero-L-gulo-heptitol
• Synonyms: 2,6-anhydro-1,3,4,5-tetra-O-benzyl-D-glycero-L-gulo-heptitol
• CAS NO: 79258-16-5
• Molecular Weight: 554.683
• Mol File: 79258-16-5.mol

Chemical Properties

• CAS DataBase Reference: 2,6-anhydro-1,3,4,5-tetra-O-benzyl-D-glycero-L-gulo-heptitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-anhydro-1,3,4,5-tetra-O-benzyl-D-glycero-L-gulo-heptitol(79258-16-5)
• EPA Substance Registry System: 2,6-anhydro-1,3,4,5-tetra-O-benzyl-D-glycero-L-gulo-heptitol(79258-16-5)

Safety Data

• Hazardous Substances Data: 79258-16-5(Hazardous Substances Data)

Upstream product

• 79258-18-7 (2R,3R,4R,5S)-1,3,4,5-tetrakis(benzyloxy)hept-6-en-2-ol 
• 113889-71-7 1-(1(Z)-octenyl)-2,3,4,6-tetra-O-benzyl-α-D-glucopyranose 
• 113794-27-7 α-1,5-anhydro-1-C-(2-phenylethynyl)-2,3,4,6-tetra-O-benzyl-D-glucitol 
• 13096-62-3 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one 
• 917-54-4 methyllithium 
• 133697-34-4 2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-deoxy-D-gluco-hept-1-enitol 
• 113794-28-8 (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-3-methoxy-1-propyne 
• 4196-36-5 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl 4-nitrobenzoate 
• 4196-35-4 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl bromide 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 113889-63-7 (2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-1-octyne 
• 113794-37-9 1-(3-methoxy-1'(Z)-propenyl)-2,3,4,6-tetra-O-benzyl-α-D-glucopyranose 
• 113794-36-8 1-(1-phenyl-2(Z)-ethylene)-2,3,4,6-tetra-O-benzyl-α-D-glucopyranose 

Downstream Products

• 89023-68-7 1,3,4,5,7-penta-2,6-anhydro-D-glycero-L-gulo-hepitol 
• 155101-37-4 2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-C-phenyl-D-glycero-D-ido-heptose 
• 155158-60-4 2,6-anhydro-3,4,5,7-tetra-O-benzyl-1-C-phenyl-D-erythro-L-ido-heptitol 
• 155101-38-5 2,6-anhydro-7-azido-1,3,4,5,-tetra-O-benzyl-7-deoxy-7-C-phenyl-D-erythro-L-guloheptitol 
• 155101-41-0 2,6-anhydro-1,3,4,5-tetra-O-benzyl-7-tert-butoxycarbonylamino-7-deoxy-7-C-phenyl-D-erythro-L-gulo-heptitol 
• 155101-42-1 2,6-anhydro-7-tert-butoxycarbonylamino-7-deoxy-7-C-phenyl-D-erythro-L-gulo-heptitol 
• 155101-40-9 7-amino-2,6-anhydro-1,3,4,5-tetra-O-benzyl-7-deoxy-7-C-phenyl-D-erythro-L-gulo-heptitol 
• 936132-16-0 1-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)formic acid 
• 136089-06-0 1-(2,3,4,6-O-tetrabenzyl-α-D-glucopyranosyl)-1(R)-deuteriopropane-2,3-(2R)-diol 2,3-thionocarbonate 
• 136172-73-1 C₃₇H₄₁⁽²⁾HO₇ 
• 136089-05-9 C₃₇H₄₁⁽²⁾HO₇ 
• 136172-71-9 (1S,2S)-1-(2,3,4,6-O-tetrabenzyl-α-D-glucopyranosyl)-1-deuteriopropane-2,3-diol 
• 136089-04-8 (1R,2R)-1-(2,3,4,6-O-tetrabenzyl-α-D-glucopyranosyl)-1-deuteriopropane-2,3-diol 
• 136088-97-6 methyl 3-(2,3,4,6-O-tetrabenzyl-α-D-glucopyranosyl)propenoate 

Relevant articles and documents

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Mercuricyclisation in Carbohydrate Chemistry: A Highly Stereoselective Route to α-D-C-Glucopyranosyl Derivatives

Mercuricyclisation of an olefin which is prepared from the carbohydrate 2,3,4,6-tetra-O-benzyl-D-glucopyranose using a Wittig reaction provides the axial chloromercuri-ether as the only isolated product, thus offering the first stereospecific route to 1,5