96690-02-7

Basic information

• Product Name: 5-O-(tert-butyldiphenylsilyl)-2,3-O-isopropylidene-D-ribofuranose
• Synonyms: 5-O-(tert-butyldiphenylsilyl)-2,3-O-isopropylidene-D-ribofuranose
• CAS NO: 96690-02-7
• Molecular Weight: 428.601
• Mol File: 96690-02-7.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 5-O-(tert-butyldiphenylsilyl)-2,3-O-isopropylidene-D-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 5-O-(tert-butyldiphenylsilyl)-2,3-O-isopropylidene-D-ribofuranose(96690-02-7)
• EPA Substance Registry System: 5-O-(tert-butyldiphenylsilyl)-2,3-O-isopropylidene-D-ribofuranose(96690-02-7)

Safety Data

• Hazardous Substances Data: 96690-02-7(Hazardous Substances Data)

Upstream product

• 532-20-7 D-Ribose 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 67814-68-0 2,3-O-isopropylidene-β-D-ribofuranose 
• 67814-68-0 2,3-O-isopropylidene-D-ribofuranose 
• 50-69-1 D-ribose 
• 10257-32-6 D-ribose 
• 13199-25-2 2,3-O-Isopropylidene-D-ribose 

Downstream Products

• 915694-38-1 (3aR,3bR,4aS,5S,5aS)-3b-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethylhexahydrocyclopropa[3,4]cyclopenta[1,2-d][1,3]dioxol-5-ol 
• 82950-51-4 3-(5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-α-D-ribofuranosyl)prop-1-ene 
• 130222-85-4 5-O-tert-butyldiphenylsilyl-2,3-O-isopropylidene-D-ribitol 
• 681853-95-2 (-)-1-[(4S,5S)-2,2-dimethyl-5-vinyl-1,3-dioxolan-4-yl]-2-(tert-butyldiphenylsilyloxy)ethan-1-one 
• 681853-92-9 (1R,4S,5S)-(+)-4,5-isopropylidenedioxy-1-(tert-butyldiphenylsilyloxymethyl)-2-cyclopenten-1-ol 
• 303963-92-0 (3aR,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-3a,6a-dihydro-4H-cyclopenta[d][1,3]dioxol-4-one 
• 72877-50-0 neplanocin A 
• 952418-12-1 (1R,4R,5S)-9-[3-(tert-butyldiphenylsilyloxymethyl)-4,5-isopropylidenedioxy-2-cyclopenten-1-yl]adenine 

Relevant articles and documents

Highly regioselective and stereoselective synthesis of C-Aryl glycosidesvianickel-catalyzedortho-C-H glycosylation of 8-aminoquinoline benzamides

C-Aryl glycosides are of high value as drug candidates. Here a novel and cost-effective nickel catalyzedortho-CAr-H glycosylation reaction with high regioselectivity and excellent α-selectivity is described. This method shows great functional group compatibility with various glycosides, showing its synthetic potential. Mechanistic studies indicate that C-H activation could be the rate-determining step.

Synthesis, biological evaluation, and molecular docking studies of deoxygenated C-glycosides as LpxC inhibitors

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