174175-00-9

Basic information

• Product Name: methyl 5-azido-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranoside
• Synonyms: methyl 5-azido-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranoside
• CAS NO: 174175-00-9
• Molecular Weight: 397.387
• Mol File: 174175-00-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 5-azido-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-azido-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranoside(174175-00-9)
• EPA Substance Registry System: methyl 5-azido-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranoside(174175-00-9)

Safety Data

• Hazardous Substances Data: 174175-00-9(Hazardous Substances Data)

Upstream product

• 35452-26-7 methyl 5-O-toluenesulfonyl-β-D-ribofuranoside 
• 4099-85-8 ((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol 
• 50610-99-6 1-O-methyl-2,3-O-isopropylidene-5-O-(methanesulfonyl)-β-D-ribofuranoside 
• 62819-24-3 methyl 5-azido-5-deoxy-2,3-O-isopropylidene-b-ribofuranoside 
• 19945-78-9 methyl 5-O-toluenesulfonyl-2,3-di-O-benzoyl-β-D-ribofuranoside 
• 35509-22-9 methyl 5-azido-5-deoxy-β-D-ribofuranoside 
• 98-88-4 benzoyl chloride 
• 7473-45-2 1-O-methyl-D-ribofuranose 

Downstream Products

• 174019-90-0 C₃₂H₂₅N₇O₉S 
• 174019-84-2 C₂₆H₂₃N₇O₇S 
• 174019-83-1 4-amino-6-bromo-5-cyano-7-(5-azido-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine 
• 174019-88-6 C₂₇H₂₀N₆O₅S 
• 174019-85-3 4-amino-5-cyano-7-(5-amino-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidine 
• 174019-86-4 C₂₆H₂₄N₆O₅S 
• 267662-02-2 methyl-5-deoxy-5-trifluoroacetylamino-2,3-di-O-benzoyl-β-D-ribofuranoside 
• 267661-99-4 1-O-acetyl-5-acetylamino-2,3-di-O-benzoyl-5-deoxy-α,β-D-ribofuranose 
• 267662-01-1 C₂₂H₂₃NO₇ 
• 174019-82-0 1-O-acetyl-5-azido-2,3-di-O-benzoyl-5-deoxy-β-D-ribofuranoside 

Relevant articles and documents

Synthesis and in vitro investigation of potential antiproliferative monosaccharide–D-secoestrone bioconjugates

The syntheses of monosaccharide–D-secoestrone conjugates are reported. They were prepared from 3-(prop-2-inyloxy)-D-secoestrone alcohol or oxime and monosaccharide azides via Cu(I)-catalyzed azide–alkyne cycloaddition reactions (CuAAC). The antiproliferat

Synthesis of 5'-fluoro-5'-deoxy- and 5'-amino-5'-deoxytoyocamycin and sangivamycin and some related derivatives

A series of 5'-substituted analogs of toyocamycin were prepared by condensation of silylated 4-amino-6-bromo-5-cyanopyrrolo[2,3-d]pyrimidine with protected 5-azido-5-deoxy- or 5-fluoro-5-deoxyribofuranose followed by debromination and deblocking. Alternatively, 5'-azido-5'-deoxytoyocamycin was prepared by azidation of toyocamycin. Conversion of the 5-nitrile function of the toyocamycin derivatives into a carboxamide or a thiocarboxamide gave the corresponding analogs of sangivamycin or thiosangivamycin while reduction of the 5'-azido-5'-deoxy nucleosides provided 5'-amino-5'-deoxy derivatives.