119803-58-6

Basic information

• Product Name: C₄₉H₅₇IO₂₅S
• CAS NO: 119803-58-6
• Molecular Weight: 1204.95
• Mol File: 119803-58-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₄₉H₅₇IO₂₅S(CAS DataBase Reference)
• NIST Chemistry Reference: C₄₉H₅₇IO₂₅S(119803-58-6)
• EPA Substance Registry System: C₄₉H₅₇IO₂₅S(119803-58-6)

Safety Data

• Hazardous Substances Data: 119803-58-6(Hazardous Substances Data)

Upstream product

• 119803-56-4 Benzoic acid (2R,3S,4R,5R,6R)-4,5-diacetoxy-6-[(2R,3R,4S,5R)-4,5-diacetoxy-2-acetoxymethyl-6-(4-iodo-phenoxy)-tetrahydro-pyran-3-yloxy]-3-trifluoromethanesulfonyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 62860-10-0 2,3,4,6-tetra-O-acetyl-1-S-acetyl-1-thio-α-D-glucopyranoside 
• 72718-62-8 1,2,3,6-tetra-O-acetyl-4-O-(2',3'-di-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranoside 
• 119803-50-8 1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-α-D-glucopyranosyl)-β-D-glucopyranose 
• 119803-55-3 Benzoic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-[(2R,3R,4S,5R)-4,5-diacetoxy-2-acetoxymethyl-6-(4-iodo-phenoxy)-tetrahydro-pyran-3-yloxy]-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester 
• 119803-53-1 1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-β-D-glucopyranose 
• 119803-51-9 Benzoic acid (2R,3R,4R,5R,6R)-4,5-diacetoxy-6-((2R,3R,4S,5R,6S)-4,5,6-triacetoxy-2-acetoxymethyl-tetrahydro-pyran-3-yloxy)-3-trifluoromethanesulfonyloxy-tetrahydro-pyran-2-ylmethyl ester 
• 119803-54-2 p-iodophenyl 2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-4-O-trichloroacetyl-α-D-galactopyranosyl)-D-glucopyranoside 
• 119803-52-0 1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-α-D-galactopyranosyl)-β-D-glucopyranose 

Relevant articles and documents

A CONVENIENT METHOD FOR S-GLYCOSIDIC BOND FORMATION. SYNTHESIS OF p-IODOPHENYL 4'-THIOMALTOTRIOSIDE AND ITS 2",3"-UNSATURATED ANALOGUE

The axial trifluoromethanesulphonate group at C-4' of acylated galactopyranosylglucopyranoside (11) was substituted by sulphur nucleophiles: selective S-deacetylation and activation of peracetylated 1-thio-α-D-glucose (12) led to p-iodophenyl 4'-thiomalto