37593-94-5

Basic information

• Product Name: 4-chloro-2-nitrophenyl benzoate
• Synonyms: 4-chloro-2-nitrophenyl benzoate
• CAS NO: 37593-94-5
• Molecular Formula: C₁₃H₈ClNO₄
• Molecular Weight: 277.65992
• Mol File: 37593-94-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-chloro-2-nitrophenyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-2-nitrophenyl benzoate(37593-94-5)
• EPA Substance Registry System: 4-chloro-2-nitrophenyl benzoate(37593-94-5)

Safety Data

• Hazardous Substances Data: 37593-94-5(Hazardous Substances Data)

Upstream product

• 89-64-5 p-chloro-o-nitrophenol 
• 98-88-4 benzoyl chloride 
• 92044-52-5 1-(benzyloxy)-4-chloro-2-nitrobenzene 

Downstream Products

• 613-90-1 benzoyl cyanide 
• 776-75-0 N-benzoylpiperidine 
• 89-64-5 p-chloro-o-nitrophenol 
• 1499-53-2 ethyl hippurate 
• 613-94-5 benzoic acid hydrazide 
• 1145-32-0 N-(N'-benzoyl-2-aminoethanoyl)-2-aminoethanoic acid 
• 1485-70-7 N-benzylbenzamide 
• 18838-10-3 N-(2-hydroxyethyl)-benzamide 
• 1009-17-2 N-(2-amino-ethyl)-benzamide 
• 614-17-5 N-ethylbenzamide 
• 13754-38-6 N-Benzoylpiperazine 
• 1468-28-6 4-benzoylmorpholine 
• 56227-56-6 (4-(2-hydroxyethyl)piperazin-1-yl)(phenyl)methanone 
• 19202-02-9 (RS)-N-benzoyl-3-methylpiperidine 

Relevant articles and documents

Kinetic study on aminolysis of 4-chloro-2-nitrophenyl X-substituted-benzoates in Acetonitrile and in 80 mol % H2O/20 mol % DMSO: Effect of medium on reactivity and reaction mechanism

A kinetic study on aminolysis of 4-chloro-2-nitrophenyl X-substituted-benzoates (6a-i) in MeCN is reported. The Hammett plot for the reactions of 6a-i with piperidine consists of two intersecting straight lines, while the Yukawa-Tsuno plot exhibits an exc

N-(2-hydroxyaryl)benzamide synthesis from 2-nitroaryl benzoates via an Indium-mediated reduction-migration reaction

A one-pot reduction-triggered N-(2-hydroxyaryl)benzamide synthesis from 2-nitroaryl benzoate substrates was investigated. In the presence of indium/AcOH in THF/H2O, 2-nitroaryl benzoates produced reasonable yields of the benzo group migrated N-

Photolysis of 2-Nitrophenyl Benzyl Ethers in Neutral and Acidic Media

2-Nitrophenyl benzyl ethers (1a-d) on irradiation afford N-benzoyl-2-aminophenols (4) as the major products.The other minor products are 2-nitrophenol (2), 4-benzyl-2-nitrophenol (3), 2-phenylbenzoxazoles (5) and 2-nitrophenyl benzoate (6).A plausible mechanism to account for the formation of various products is discussed.