226919-63-7

Basic information

• Product Name: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside phosphate
• Synonyms: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside phosphate
• CAS NO: 226919-63-7
• Molecular Weight: 726.844
• Mol File: 226919-63-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside phosphate(226919-63-7)
• EPA Substance Registry System: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside phosphate(226919-63-7)

Safety Data

• Hazardous Substances Data: 226919-63-7(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 604767-65-9 Phosphoric acid (4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yl ester dibutyl ester 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 107-66-4 dibutyl phosphate 
• 1011723-04-8 glucal epoxide 

Downstream Products

• 226919-73-9 thioethyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside-(1->6)-3,4-di-O-benzyl-2-O-pivaloyl-β-D-mannopyranoside 
• 373606-44-1 dibutyl 3,4,6-tri-O-benzyl-2-O-pivaloyl-β-D-glucopyranosyl-(1->6)-3,4-O-carbonyl-2-O-pivaloyl-α-D-galactopyranoside phosphate 
• 1177256-99-3 C₃₉H₅₀O₇ 
• 340177-72-2 2,2-Dimethyl-propionic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-{(2R,3R,4S,5R,6R)-3,4-bis-benzyloxy-6-methoxy-5-[4-(methyl-phenyl-amino)-benzyloxy]-tetrahydro-pyran-2-ylmethoxy}-tetrahydro-pyran-3-yl ester 
• 294637-53-9 methyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-glucopyranoside-(1->6)-3,4-di-O-benzyl-2-O-(4-chlorobenzyl)-β-D-glucopyranoside 

Relevant articles and documents

Synthesis and use of glycosyl phosphates as glycosyl donors

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Oligosaccharide synthesis with glycosyl phosphate and dithiophosphate triesters as glycosylating agents

Described is an efficient one-pot synthesis of α- and β-glycosyl phosphate and dithiophosphate triesters from glycals via 1,2-anhydrosugars. Glycosyl phosphates function as versatile glycosylating agents for the synthesis of β-glucosidic, β-galactosidic,

Halobenzyl ethers as protecting groups for organic synthesis [18]

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