331281-75-5

Basic information

• Product Name: 3,4,6-Tri-O-benzyl-2-para-chlorophenylcarbonyl-β-D-glucopyranosyl-(1->6)-1,2:3,4-diisopropylidene-α-D-galactopyranoside
• Synonyms: 3,4,6-Tri-O-benzyl-2-para-chlorophenylcarbonyl-β-D-glucopyranosyl-(1->6)-1,2:3,4-diisopropylidene-α-D-galactopyranoside
• CAS NO: 331281-75-5
• Molecular Weight: 847.356
• Mol File: 331281-75-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,4,6-Tri-O-benzyl-2-para-chlorophenylcarbonyl-β-D-glucopyranosyl-(1->6)-1,2:3,4-diisopropylidene-α-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,6-Tri-O-benzyl-2-para-chlorophenylcarbonyl-β-D-glucopyranosyl-(1->6)-1,2:3,4-diisopropylidene-α-D-galactopyranoside(331281-75-5)
• EPA Substance Registry System: 3,4,6-Tri-O-benzyl-2-para-chlorophenylcarbonyl-β-D-glucopyranosyl-(1->6)-1,2:3,4-diisopropylidene-α-D-galactopyranoside(331281-75-5)

Safety Data

• Hazardous Substances Data: 331281-75-5(Hazardous Substances Data)

Upstream product

• 208656-41-1 Phosphoric acid (2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yl ester dibutyl ester 
• 180187-58-0 ethyl 3,4,6-tri-O-benzyl-1-thio-β-D-glucopyranoside 
• 74372-90-0 3,4,6-tri-O-benzyl-D-glucal epoxide 
• 7693-45-0 4-Chlorophenyl chloroformate 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 4064-06-6 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose 
• 331281-73-3 Dibutyl 3,4,6-tri-O-benzyl-2-O-para-chlorophenylcarbonyl-β-D-glucipyranosyl phosphate 
• 331281-74-4 Thioethyl 3,4,6-tri-O-benzyl-2-O-para-chlorophenylcarbonyl-β-D-glucopyranoside 

Downstream Products

• 40246-33-1 3,4,6-tri-O-benzyl-β-D-glucopyranoside-(1->6)-1,2:3,4-di-O-isopropylidene-α-D-galactopyranoside 

Relevant articles and documents

para-Chlorophenyl carbonate as a versatile hydroxyl protecting group

The p-chlorophenyl carbonate (CPC) group can be readily applied and rapidly removed in the presence of various protecting groups including pivaloyl and benzoyl esters. Additionally, the CPC group is stable under a variety of glycosylation conditions and yields solely β-linked glycosides when used as a C2 participating group.