76479-97-5

Basic information

• Product Name: methyl 2,3-O-isopropylidene-5-O-(p-nitrobenzoyl)-β-D-ribofuranoside
• Synonyms: methyl 2,3-O-isopropylidene-5-O-(p-nitrobenzoyl)-β-D-ribofuranoside
• CAS NO: 76479-97-5
• Molecular Weight: 353.329
• Mol File: 76479-97-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2,3-O-isopropylidene-5-O-(p-nitrobenzoyl)-β-D-ribofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,3-O-isopropylidene-5-O-(p-nitrobenzoyl)-β-D-ribofuranoside(76479-97-5)
• EPA Substance Registry System: methyl 2,3-O-isopropylidene-5-O-(p-nitrobenzoyl)-β-D-ribofuranoside(76479-97-5)

Safety Data

• Hazardous Substances Data: 76479-97-5(Hazardous Substances Data)

Upstream product

• 4099-85-8 ((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol 
• 122-04-3 4-nitro-benzoyl chloride 

Downstream Products

• 6427-66-3 4-azidobenzoic acid 
• 76480-02-9 4-Amino-benzoic acid (3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 
• 76479-98-6 4-Azido-benzoic acid (3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 
• 76480-00-7 C₃₂H₃₈N₂O₁₂ 
• 62-23-7 4-nitro-benzoic acid 

Relevant articles and documents

Competing SNAr displacements of nitrite and SN2 displacements on the alkyl groups of alkyl p-nitrobenzoates and o-nitrobenzoates

Several p-nitrobenzoate and o-nitrobenzoate esters have been found to undergo competing SNAr and SN2 reactions with azide, alkoxide, and thiophenoxide ions. SNAr displacement of the nitro group even competes with SN2 displacement on the methyl group of methyl esters 1c and 11. Esters 1a and 1b undergo predominately SNAr displacements with azide, whereas 1c undergoes predominately an SN2 displacement with azide. Both 1b and 1c undergo predominately SNAr reactions with alkoxides and thiophenoxide. The SNAr products from the azide reactions consist of mixtures of p-azidobenzoates, p-aminobenzoates, and 4,4′-azodibenzoates whose compositions depend upon the reaction conditions.