34662-29-8

Basic information

• Product Name: 3-Chloro-4-nitrobenzonitrile
• Synonyms: 3-Chloro-4-nitrobenzonitrile
• CAS NO: 34662-29-8
• Molecular Formula: C₇H₃ClN₂O₂
• Molecular Weight: 182.56392
• Mol File: 34662-29-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 319.7±27.0 °C(Predicted)
• Appearance: /
• Density: 1.47±0.1 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-Chloro-4-nitrobenzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloro-4-nitrobenzonitrile(34662-29-8)
• EPA Substance Registry System: 3-Chloro-4-nitrobenzonitrile(34662-29-8)

Safety Data

• Hazardous Substances Data: 34662-29-8(Hazardous Substances Data)

Usage

General Description

3-Chloro-4-nitrobenzonitrile is a chemical compound with the molecular formula C7H3ClN2O2. It is a yellow crystalline solid that is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is primarily used as a building block in the production of organic compounds for various industrial applications. 3-Chloro-4-nitrobenzonitrile is a nitroaromatic compound that is considered toxic and should be handled with care to avoid exposure. It is also important to note that this compound may pose environmental risks and should be disposed of properly according to regulations.

Upstream product

• 825-41-2 3-chloro-4-nitroaniline 
• 21803-75-8 4-amino-3-chlorobenzonitrile 
• 1317-39-1 copper(I) oxide 

Downstream Products

• 467235-08-1 3-(ethylamino)-4-nitrobenzonitrile 
• 21803-75-8 4-amino-3-chlorobenzonitrile 
• 1393176-18-5 4-nitro-3-N-(phenylamino)benzonitrile 
• 64910-48-1 3-N-(methylamino)-4-nitrobenzonitrile 
• 467235-09-2 4-amino-3-ethylamino-benzonitrile 
• 467235-11-6 3-ethyl-3H-benzotriazole-5-carboxylic acid methyl ester 
• 857283-87-5 1,4-dimethyl-1,2,3,4-tetrahydroquinoxaline-6-carbonitrile 
• 1301189-97-8 3-({[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]methyl}amino)-4-nitrobenzonitrile 
• 918796-53-9 C₁₁H₁₃N₃O₂ 
• 438564-52-4 4-ethylamino-3-chloro benzonitrile 
• 889884-86-0 C₁₁H₁₃N₃O₃ 
• 773884-04-1 4-nitro-3-[(2-phenylethyl)amino]benzonitrile 
• 773884-34-7 2-oxo-3-(2-phenylethyl)-2,3-dihydro-1H-benzimidazole-5-carbonitrile 

Relevant articles and documents

Phenylpiperazine derivatives with a combination of partial dopamine-D2 receptor agonism and serotonin reuptake inhibition

The invention relates to a group of novel phenylpiperazine derivatives with a dual mode of action: serotonin reuptake inhibition and partial agonism on dopamine-D2 receptors. The invention also relates to the use of a compound disclosed herein for the manufacture of a medicament giving a beneficial effect. The compounds have the general formula (1): wherein the symbols have the meanings given in the specification. and tautomers, stereoisomers and N-oxides thereof, as well as pharmacologically acceptable salts, hydrates and solvates of said compounds of formula (1) and its tautomers, stereoisomers and N-oxides.

Novel benzotriazoles anti-inflammatory compounds

The present invention relates to novel benzotriazoles of the formula I wherein Het is an optionally substituted 5-membered heterocycle containing one to two heteroatoms selected from nitrogen, sulfur and oxygen wherein at least one of said heteroatoms ato

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Various 2'-phenoxymethanesulfonanilide derivatives were synthesized and evaluated for antiinfiammatory and analgesic activities. Some compounds bearing an electron-attracting substituent at the 4'-position strongly inhibited adjuvant-induced arthritis in rats and acetic acid-induced writhing syndrome in mice without causing gastro-intestinal irritation. Among them, 4'-cyano-(FK867) and 4'-acetyl-(FK3311) 2'-(2,4-difluorophenoxy)methanesulfonanilides were selected as the candidates for further development.