70849-14-8

Basic information

• Product Name: 1-O-dihydrocholesterolyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• Synonyms: 1-O-dihydrocholesterolyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside
• CAS NO: 70849-14-8
• Molecular Weight: 911.318
• Mol File: 70849-14-8.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 1-O-dihydrocholesterolyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-dihydrocholesterolyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(70849-14-8)
• EPA Substance Registry System: 1-O-dihydrocholesterolyl-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside(70849-14-8)

Safety Data

• Hazardous Substances Data: 70849-14-8(Hazardous Substances Data)

Upstream product

• 80-97-7 Cholestanol 
• 130948-37-7 C₅₃H₅₂NO₈PS 
• 143520-19-8 C₃₈H₄₇N₂O₇P 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 80-97-7 3-β-cholestanol 
• 78153-79-4 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl fluoride 
• 80300-30-7 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 42995-55-1 3-β-cholestanyl trimethylsilyl ether 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 96863-21-7 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl dimethylphosphinothioate 
• 92414-01-2 Dichloro-acetic acid (2S,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl ester 
• 100-44-7 benzyl chloride 
• 19459-10-0 3β-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-5α-cholestan 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 

Relevant articles and documents

Tandem catalysis strategy for direct glycosylation of 1-hydroxy sugars. Methoxyacetic acid as an effective catalytic mediator

1-Hydroxy sugars were dehydratively coupled with a variety of alcohols including thiophenol in the presence of a catalytic amount of ytterbium(III) triflate [Yb(OTf)3] and methoxyacetic acid to give the corresponding glycosides in good to excel

Cationic palladium(II)-catalyzed stereoselective glycosylation with glycosyl trichloroacetimidates

(Chemical Equation Presented) The development of a new method for stereoselective glycosylation with glycosyl trichloroacetimidate donors employing cationic palladium(II), Pd(CH3CN)4(BF 4)2, is described. This p

BF3·OEt2 enhanced Yb(OTf)3-promoted glycosidation of 1-O-acyl-D-glucopyranose 1

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