1370590-24-1

Basic information

• Product Name: 2-allylphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside
• Synonyms: 2-allylphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside
• CAS NO: 1370590-24-1
• Molecular Weight: 656.819
• Mol File: 1370590-24-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-allylphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-allylphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(1370590-24-1)
• EPA Substance Registry System: 2-allylphenyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside(1370590-24-1)

Safety Data

• Hazardous Substances Data: 1370590-24-1(Hazardous Substances Data)

Upstream product

• 83-87-4 D-Mannose pentaacetate 
• 1370590-22-9 2-allylphenyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 1745-81-9 o-Allylphenol 

Downstream Products

• 3879-79-6 (2R,3R,4S,5S,6S)-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)-6-methoxytetrahydro-2H-pyran 
• 1370590-34-3 4-O-acetyl-1,6-anhydro-3-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-gulopyranose 
• 55094-26-3 methyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1→6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 64694-18-4 methyl 4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)(1→4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside 
• 25018-28-4 2,3,4,6-tetrabenzyl-α-D-mannopyranosyl-(1->1)-2,3,4,6-tetrabenzyl-α-D-mannopyranoside 
• 1370590-32-1 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-N-tert-butoxycarbonyl-L-serine tert-butyl ester 
• 89615-39-4 benzyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside 
• 881198-69-2 1,6-anhydro-2-O-benzoyl-3-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-β-L-idopyranose 
• 1451154-35-0 C₄₄H₄₉NO₆ 

Relevant articles and documents

2-Allylphenyl glycosides as glycosyl donors for sugar coupling

Glycosylations employing 2-allylphenyl glycoside, a new type of stable glycosyl donor, were optimized and explored with a variety of acceptors promoted by ICl/AgOTf. The utility of the protocol was further demonstrated with an efficient synthesis of the disaccharide fragment of bleomycins.