74808-16-5

Basic information

• Product Name: (1R,2S,6S,7R,8R)-4,4-Dimethyl-7-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane
• Synonyms: (1R,2S,6S,7R,8R)-4,4-Dimethyl-7-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane
• CAS NO: 74808-16-5
• Molecular Weight: 724.848
• Mol File: 74808-16-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1R,2S,6S,7R,8R)-4,4-Dimethyl-7-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S,6S,7R,8R)-4,4-Dimethyl-7-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane(74808-16-5)
• EPA Substance Registry System: (1R,2S,6S,7R,8R)-4,4-Dimethyl-7-((2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecane(74808-16-5)

Safety Data

• Hazardous Substances Data: 74808-16-5(Hazardous Substances Data)

Upstream product

• 130948-37-7 C₅₃H₅₂NO₈PS 
• 17073-95-9 (2S,6R,7R,8S)-4,4-Dimethyl-3,5,9,11-tetraoxa-tricyclo[6.2.1.0^2,6]undecan-7-ol 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 79386-43-9 diphenyl 2,3,4,6-tetra-O-benzyl-α-D-glucosyl phosphate 
• 52579-97-2 1,6-anhydro-3,4-O-isopropylidene-β-D-galactopyranose 
• 166733-02-4 S-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-N,N,N',N'-tetramethyl-N''-phenylphosphorodiamidimidothioate 
• 129823-34-3 C₅₃H₅₂NO₈PS 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 

Relevant articles and documents

An efficient construction of 1,2-trans-β-glycosidic linkages via benzyl-protected glycopyranosyl P,P-diphenyl-N-(p-toluenesulfonyl)phosphinimidates

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A MILD AND RAPID 1,2-TRANS-GLYCOSIDATION METHOD VIA BENZOYL-PROTECTED GLYCOPYRANOSYL P,P-DIPHENYL-N-(p-TOLUENESULFONYL)PHOSPHINIMIDATES

A highly efficient 1,2-trans-glycosidation reaction with a range of acid-labile alcohols has been developed by employing benzoyl-protected glycopyranosyl P,P-diphenyl-N-(p-toluenesulfonyl)phosphinimidates as glycosyl donors.

Einfache Synthese von α- und β-O-Glykosylimidaten; Herstellung von Glykosiden und Disacchariden

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