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
• Article Data: 2

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

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.