156325-61-0

Basic information

• Product Name: allyl 4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside
• Synonyms: allyl 4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside
• CAS NO: 156325-61-0
• Molecular Weight: 536.857
• Mol File: 156325-61-0.mol

Chemical Properties

• CAS DataBase Reference: allyl 4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside(156325-61-0)
• EPA Substance Registry System: allyl 4,6-O-benzylidene-2,3-bis-O-(tert-butyldimethylsilyl)-β-D-glucopyranoside(156325-61-0)

Safety Data

• Hazardous Substances Data: 156325-61-0(Hazardous Substances Data)

Upstream product

• 48149-74-2 allyl D-glucopyranoside 
• 2280-44-6 D-Glucose 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 20746-64-9 allyl (R)-4,6-O-benzylidene-β-D-gluco-pyranoside 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 156325-70-1 2-oxopropyl 4-O-benzyl-3-O-carbamoyl-2-O-(N-acetylglycyl)-β-D-glucopyranosiduronamide 
• 156325-69-8 allyl 4-O-benzyl-3-O-carbamoyl-2-O-(N-acetylglycyl)-β-D-glucopyranosiduronamide 
• 156325-64-3 allyl 4-O-benzyl-2,3-di-O-t-butyldimethylsilyl-β-D-glucopyranosiduronamide 
• 156325-63-2 allyl 4-O-benzyl-2,3-di-O-t-butyldimethylsilyl-β-D-glucopyranosiduronic acid 
• 156325-67-6 allyl 4-O-benzyl-2-O-t-butyldimethylsilyl-3-O-carbamoyl-β-D-glucopyranosiduronamide 
• 156325-68-7 allyl 4-O-benzyl-3-O-carbamoyl-β-D-glucopyranosiduronamide 
• 156325-65-4 allyl 4-O-benzyl-2-O-t-butyldimethylsilyl-β-D-glucopyranosiduronamide 
• 156325-62-1 allyl 4-O-benzyl-2,3-di-O-t-butyldimethylsilyl-β-D-glucopyranoside 

Relevant articles and documents

Synthesis of the AB-ring segment for the convergent construction of the left half in ciguatoxin

The synthesis of the AB-ring segment aiming at the convergent construction of the left half in ciguatoxin (CTX1B) has been achieved by a strategy based on ring-closing metathesis (RCM) and diastereocontrolled hydroboration to cyclic vinyl ethers.

Structural analogues of the antibiotic moenomycin a with a D-glucose-derived unit F

Disaccharide derivative 1a is the smallest transglycosylase inhibiting compound known up to now. Structurally closely related compounds 11b and 19c have been synthesized. They do not inhibit the transglycosylase demonstrating the high specificity of the interaction between inhibitor 1a and the binding-site at the enzyme.