51130-02-0

Basic information

• Product Name: cyano(4-nitrophenyl)methyl benzoate
• CAS NO: 51130-02-0
• Molecular Formula: C₁₅H₁₀N₂O₄
• Molecular Weight: 282.2509
• Mol File: 51130-02-0.mol

Chemical Properties

• Boiling Point: 486.5°C at 760 mmHg
• Flash Point: 248°C
• Density: 1.34g/cm³
• Vapor Pressure: 1.29E-09mmHg at 25°C
• Refractive Index: 1.616
• CAS DataBase Reference: cyano(4-nitrophenyl)methyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: cyano(4-nitrophenyl)methyl benzoate(51130-02-0)
• EPA Substance Registry System: cyano(4-nitrophenyl)methyl benzoate(51130-02-0)

Safety Data

• Hazardous Substances Data: 51130-02-0(Hazardous Substances Data)

Upstream product

• 151-50-8 potassium cyanide 
• 555-16-8 4-nitrobenzaldehdye 
• 98-88-4 benzoyl chloride 

Downstream Products

• 69001-69-0 4-(p-nitrobenzoyl)-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine 
• 89549-70-2 6-anilino-4-(p-nitrophenyl)-5-pyrimidinecarbonitrile 
• 89549-86-0 4-(p-nitrophenyl)-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine 
• 102034-64-0 2-benzoyloxy-1,2-bis(4-nitrophenyl)ethanone 
• 99933-51-4 Benzoic acid cyano-(4-nitro-phenyl)-quinazolin-4-yl-methyl ester 
• 514197-15-0 2,3-bis(4-nitrophenyl)quinoxaline-6-carboxylic acid 
• 514197-13-8 2,3-bis(4-aminophenyl)quinoxaline-6-carboxylic acid 
• 6067-45-4 4,4'-dinitrobenzil 
• 102034-66-2 2-benzoyloxy-1(4-nitrophenyl)-2-phenylethanone 
• 89549-85-9 Benzoic acid cyano-(4-nitro-phenyl)-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-methyl ester 

Relevant articles and documents

Room-temperature free-radical-induced polymerization of 1,1′-(methylenedi-1,4-phenylene)bismaleimide via a novel diphenylquinoxaline-containing hyperbranched aromatic polyamide

Two new diphenylquinoxaline-containing AB2 monomers, 2,3-bis(4-aminophenyl)quinoxaline-6-carboxylic acid, 5 and 2,3-bis[4-(4-aminophenoxy)phenyl]quinoxaline-6-carboxylic acid, 9 were prepared and polymerized via the Yamazaki reaction to form th

CYANOHYDRINS AS SUBSTRATES IN BENZOIN CONDENSATION. REGIOCONTROLLED MIXED BENZOIN CONDENSATION

O-Benzoylated cyanohydrins of aromatic aldehydes have been used as one of the substrates in the benzoin condensation.They were treated with aromatic aldehydes under phase-transfer conditions to result in benzoin benzoates.By this method aldehydes which fail to undergo condensation using traditional conditions could be converted into benzoins.By the Umpolung of reactivity of the pertinent aldehyde it was possible to prepare both isomeric unsymmetrical benzoins, including the thermodynamically less stable ones.

Studies on Pyrazolopyrimidine Derivatives. XIII. Aryl Migration of 4-Aroyl-1H-pyrazolopyrimidines to 4-Aryl-4,5-dihydro-1H-pyrazolopyrimidine-4-carboxylic Acids

When a mixture of 4-aroyl-1-phenyl-1H-pyrazolopyrimidines (3) and sodium hydroxide in dimethyl sulfoxide (DMSO) was stirred for 1 h at room temperature, migration of the aryl group to the 4-position occurred, i.e., the benzilic acid rearrangement,