115141-23-6

Basic information

• Product Name: 1-deoxy-1-diethylmethylsilyloxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose
• Synonyms: 1-deoxy-1-diethylmethylsilyloxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose
• CAS NO: 115141-23-6
• Molecular Weight: 576.719
• Mol File: 115141-23-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-deoxy-1-diethylmethylsilyloxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 1-deoxy-1-diethylmethylsilyloxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose(115141-23-6)
• EPA Substance Registry System: 1-deoxy-1-diethylmethylsilyloxymethyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose(115141-23-6)

Safety Data

• Hazardous Substances Data: 115141-23-6(Hazardous Substances Data)

Upstream product

• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 760-32-7 diethylmethylsilane 
• 201230-82-2 carbon monoxide 

Downstream Products

• 1315073-28-9 C₂₀H₂₃IN₆O₄ 
• 1315073-26-7 C₂₃H₂₇IN₆O₄ 
• 1315073-27-8 C₁₉H₂₁IN₆O₄ 
• 1315073-25-6 C₂₂H₂₅IN₆O₄ 
• 1315073-24-5 C₂₁H₂₂IN₅O₅ 
• 1315073-23-4 C₂₁H₂₄IN₅O₄ 
• 1315073-22-3 C₁₈H₂₀IN₅O₄ 
• 1315073-21-2 C₃₉H₃₂IN₅O₇ 
• 561017-92-3 2,5-anhydro-3,4,6-tri-O-benzoyl-1-O-butyldiphenylsilyl-D-allitol 
• 561018-00-6 2,5-anhydro-1-O-tert-butyldiphenylsilyl-3,4-O-isopropylidene-5-C-mesyloxymethyl-6-O-mesyl-D-allitol 
• 561018-02-8 2,5-anhydro-1-O-tert-butyldiphenylsilyl-5-C-mesyloxymethyl-6-O-mesyl-D-allitol 
• 561017-56-9 2,5-anhydro-3,4,6-tri-O-benzoyl-1-O-mesyl-D-allitol 
• 561018-08-4 2,5-anhydro-6-tert-butoxycarbonylamino-1-O-tert-butyldiphenylsilyl-6-deoxy-4-O,5-C-methylene-D-allitol 
• 561017-59-2 2,5-anhydro-1-azido-3,4,6-tri-O-benzoyl-1-deoxy-D-allitol 

Relevant articles and documents

STEREOCHEMICAL ASPECTS OF CATALYTIC SILOXYMETHYLATION OF VARIOUS OXYGEN-CONTAINING COMPOUNDS WITH HYDROSILANES AND CARBON MONOXIDE IN THE PRESENCE OF DICOBALT OCTACARBONYL

Siloxymethylation of oxygen-containing compounds by a new catalytic reaction, HSiR3/CO/Co2(CO)8, is described with emphasis laid on stereoselectivity.In the catalytic reaction, the carbon-oxygen bond in the substrates is cleaved and displaced by a trialky

Synthesis and binding affinity of homologated adenosine analogues as A3 adenosine receptor ligands

Homologated analogues 3a and 3b of potent and selective A3 adenosine receptor ligands, IB-MECA and dimethyl-IB-MECA were synthesized from commercially available 1-O-acetyl-2,3,5-tri-O-benzoyl-β-Dribofuranose (4) via Co2(CO)8-catalyze