220903-24-2

Basic information

• Product Name: Benzoic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-hydroxymethyl-2-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl ester
• Synonyms: Benzoic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-hydroxymethyl-2-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl ester
• CAS NO: 220903-24-2
• Molecular Weight: 911.058
• Mol File: 220903-24-2.mol

Chemical Properties

• CAS DataBase Reference: Benzoic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-hydroxymethyl-2-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-hydroxymethyl-2-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl ester(220903-24-2)
• EPA Substance Registry System: Benzoic acid (2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-hydroxymethyl-2-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl ester(220903-24-2)

Safety Data

• Hazardous Substances Data: 220903-24-2(Hazardous Substances Data)

Upstream product

• 220903-20-8 1,6-di-O-acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranose 
• 40246-29-5 methyl 2-O-benzoyl-3,4,6-tetra-O-benzyl-α-D-mannopyranoside 
• 34212-64-1 methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 220903-23-1 Benzoic acid (2S,3S,4S,5R,6R)-6-acetoxymethyl-4,5-bis-benzyloxy-2-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-3-yl ester 

Relevant articles and documents

Facile syntheses of a hexasaccharide and a nonasaccharide related to the cell wall D-mannan of yeast Candida albicans

A highly efficient strategy for the preparation of D-manno-hexa- and nonasaccharides related to the cell wall D-mannan of yeast Candida albicans having α-(1→6)- and α-(1→2)-linkages has been developed using 6-O- acetyl-2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl trichloroacetimidate (7) as the key glycosyl donor in the 'Inverse Schmidt' procedure.