155896-88-1

Basic information

• Product Name: Allyl 2-O-Benzoyl-4,6-O-benzylidene-α-D-glucopyranoside
• Synonyms: Allyl 2-O-Benzoyl-4,6-O-benzylidene-α-D-glucopyranoside
• CAS NO: 155896-88-1
• Molecular Weight: 412.439
• Mol File: 155896-88-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Allyl 2-O-Benzoyl-4,6-O-benzylidene-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl 2-O-Benzoyl-4,6-O-benzylidene-α-D-glucopyranoside(155896-88-1)
• EPA Substance Registry System: Allyl 2-O-Benzoyl-4,6-O-benzylidene-α-D-glucopyranoside(155896-88-1)

Safety Data

• Hazardous Substances Data: 155896-88-1(Hazardous Substances Data)

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 54769-36-7 N-benzoyloxybenzotriazole 
• 7464-56-4 1-O-allyl-α-D-glucopyranoside 
• 2280-44-6 D-Glucose 
• 65987-12-4 1-O-allyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 98-88-4 benzoyl chloride 
• 4231-62-3 1-benzoyl-1H-benzotriazole 

Downstream Products

• 127446-66-6 Allyl 2,6-Di-O-benzoyl-3,4-di-O-methylsulfonyl-α-D-glucopyranoside 
• 127446-69-9 Benzoic acid (2S,3R,4R,5R,6R)-2-allyloxy-6-(tert-butyl-dimethyl-silanyloxymethyl)-4,5-bis-methanesulfonyloxy-tetrahydro-pyran-3-yl ester 
• 127446-71-3 Allyl 2,6-di-O-benzoyl-α-D-glucopyranoside 
• 1053721-74-6 C₆₁H₆₀O₁₆ 
• 127446-68-8 Allyl 2-O-Benzoyl-α-D-glucopyranoside 
• 155786-73-5 allyl O-(2,3,4-tri-O-benzoyl-α-D-glucopyranosyl)-(1<*>2)-O-(3,4,6-tri-O-acetyl-α-D-glucopyranosyl)-(1<*>3)-2-O-benzoyl-4,6-benzylidene-α-D-glucopyranoside 

Relevant articles and documents

Synthesis of An Elicitor-Active Hexaglucoside Analogue by a One-Pot, Two-Step Glycosidation Procedure

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Regioselective acylation of carbohydrates with 1-acyloxy-1H-benzotriazoles

Acylation of representative carbohydrate derivatives was accomplished with in situ generated 1-acyloxy-1H-benzotriazoles. The observed high regioselectivity, mild reaction conditions and convenient work-up make the presented one-pot procedure generally applicable and more advantageous than acylations with previously introduced reagents, including N-acylimidazoles.