59202-80-1

Basic information

• Product Name: Acetic acid (2R,3R,4S,5R)-4,5-diacetoxy-6-bromo-2-(toluene-4-sulfonyloxymethyl)-tetrahydro-pyran-3-yl ester
• Synonyms: Acetic acid (2R,3R,4S,5R)-4,5-diacetoxy-6-bromo-2-(toluene-4-sulfonyloxymethyl)-tetrahydro-pyran-3-yl ester
• CAS NO: 59202-80-1
• Molecular Weight: 523.356
• Mol File: 59202-80-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Acetic acid (2R,3R,4S,5R)-4,5-diacetoxy-6-bromo-2-(toluene-4-sulfonyloxymethyl)-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (2R,3R,4S,5R)-4,5-diacetoxy-6-bromo-2-(toluene-4-sulfonyloxymethyl)-tetrahydro-pyran-3-yl ester(59202-80-1)
• EPA Substance Registry System: Acetic acid (2R,3R,4S,5R)-4,5-diacetoxy-6-bromo-2-(toluene-4-sulfonyloxymethyl)-tetrahydro-pyran-3-yl ester(59202-80-1)

Safety Data

• Hazardous Substances Data: 59202-80-1(Hazardous Substances Data)

Upstream product

• 530-26-7 D-Mannose 
• 95118-61-9 1,2,3,4-tetra-O-acetyl-6-O-p-tolylsulfonyl-α,β-D-glucopyranose 
• 23661-33-8 methyl 2,3,4-tri-O-acetyl-6-O-(p-tolylsulfonyl)-α-D-glucopyranoside 
• 20113-43-3 1,2,3,4-tetra-O-acetyl-6-O-p-tolylsulfonyl-α-D-glucopyranose 
• 103042-48-4 3,4-di-O-acetyl-2,6-di-O-tosyl-α/β-D-glucopyranose 
• 98-59-9 p-toluenesulfonyl chloride 
• 78478-66-7 1,2,3,4-tetra-O-acetyl-6-O-deoxy-6-tosyl-α/β-D-mannopyranose 
• 50-99-7 D-glucose 
• 6619-07-4 6-O-p-toluenesulfonyl-D-mannopyranose 

Downstream Products

• 69240-09-1 2,3,4-tri-O-acetyl-1,5-anhydro-6-O-(4-methylphenylsulfonyl)-D-arabino-hex-1-enitol 
• 871011-08-4 2,3,4-tri-O-acetyl-1-S-methylsulfonyl-6-O-(4-methylphenylsulfonyl)-1-thio-β-D-glucose 
• 1206797-11-6 C₂₀H₂₆O₁₁S 
• 1207854-30-5 C₂₁H₂₈O₁₁S 
• 1206797-14-9 C₂₂H₂₆O₁₁S 
• 1333231-24-5 (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-carboxymethyl-3,4-di-O-benzoyl-6-azido-α-D-mannopyranose 
• 1333231-19-8 (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4-di-O-benzoyl-6-azido-α-D-mannopyranose 
• 1333231-22-3 (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-carboxylmethyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose 
• 1333231-18-7 (2,3,4-tri-O-acetyl-6-azido-α-D-mannopyranosyl)-(1->2)-allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranose 
• 1333231-21-2 (2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->2)-carboxymethyl-3,4-di-O-benzoyl-6-azido-α-D-mannopyranose 
• 1333231-17-6 (2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-(1->2)-allyl-3,4-di-O-benzoyl-6-azido-α-D-mannopyranose 
• 1333231-14-3 allyl 3,4-di-O-benzoyl-6-azido-α-D-mannopyranoside 
• 1333231-13-2 allyl 2-O-acetyl-3,4-di-O-benzoyl-6-azido-α-D-mannopyranoside 
• 1333231-12-1 1,2-di-O-acetyl-3,4-di-O-benzoyl-6-azido-α-D-mannopyranoside 

Relevant articles and documents

Selection of a synthetic glycan oligomer from a library of DNA-templated fragments against DC-SIGN and inhibition of HIV gp120 binding to dendritic cells

We report the synthesis of a nucleic acid-encoded carbohydrate library, its combinatorial self-assembly into 37485 pairs and a screen against DC-SIGN leading to the identification of consensus ligand motifs. A prototypical example from the selected pairs

Synthesis of the bicyclic core of tagetitoxin

A synthesis of the 9-oxa-3-thiabicyclo[3.3.1]nonane ring system, which constitutes the core of the RNA polymerase inhibitor tagetitoxin, has been achieved through cyclisation of a thiol onto an electrophilic ketone. The Royal Society of Chemistry 2006.

Structure-Activity Relationships of β-D-(2S,5R)- and α-D-(2S,5S)-1,3-oxathiolanyl Nucleosides as Potential Anti-HIV Agents

The β-D-(2S,5R)- and α-D-(2S,5S)-1,3-oxathiolanylpyrimidine and -purine nucleosides with natural nucleoside configuration were synthesized and evaluated against HIV-1 in human peripheral blood mononuclear (PBM) cells.The key intermediate 14, which was uti