81713-34-0

Basic information

• Product Name: Allyl 2,6-di-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside
• Synonyms: Allyl 2,6-di-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside
• CAS NO: 81713-34-0
• Molecular Weight: 440.536
• Mol File: 81713-34-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Allyl 2,6-di-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Allyl 2,6-di-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(81713-34-0)
• EPA Substance Registry System: Allyl 2,6-di-O-benzyl-3,4-O-isopropylidene-α-D-galactopyranoside(81713-34-0)

Safety Data

• Hazardous Substances Data: 81713-34-0(Hazardous Substances Data)

Upstream product

• 104477-35-2 (3aS,4R,6S,7R,7aR)-6-Allyloxy-4-(1-methoxy-1-methyl-ethoxymethyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-ol 
• 3646-73-9 α-D-galactopyranose 
• 48149-72-0 (2S,3R,4S,5R,6R)-2-Allyloxy-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 
• 100-39-0 benzyl bromide 
• 81713-32-8 allyl 3,4-O-isopropylidene-α-D-galactopyranoside 
• 10257-28-0 D-Galactose 

Downstream Products

• 81713-36-2 allyl 4-O-benzoyl-2,6-di-O-benzyl-3-O-(2-methoxyethoxy)methyl-α-D-galactopyranoside 
• 81713-37-3 allyl 2,4,6-tri-O-benzyl-3-O-(2-methoxyethoxy)methyl-α-D-galactopyranoside 
• 81713-35-1 allyl 2,6-di-O-benzyl-3-O-(2-methoxyethoxy)methyl-α-D-galactopyranoside 
• 61236-87-1 allyl 2,4,6-tri-O-benzyl-α-D-galactopyranoside 
• 607720-98-9 allyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl-(1->3)-2,6-di-O-benzyl-α-D-galactopyranoside 
• 37111-91-4 allyl 2,6-di-O-benzyl-α-D-galactopyranoside 
• 149001-83-2 Allyl 2,6-di-O-benzyl-3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-α-D-galactopyranoside 

Relevant articles and documents

Carbohydrate-derived iminium salt organocatalysts for the asymmetric epoxidation of alkenes

A new family of carbohydrate-based dihydroisoquinolinium salts has been prepared and tested for potential as asymmetric catalysts for the epoxidation of unfunctionalized alkene substrates, providing up to 57% ee in the product epoxides.

Synthesis of an intermediate fragment of the capsular polysaccharides of Klebsiella type 8

-