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3-Chloro-4-nitrobenzonitrile is a chemical compound characterized by its molecular formula C7H3ClN2O2. It is a yellow crystalline solid known for its role as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. This nitroaromatic compound is recognized for its potential toxicity and requires careful handling to prevent exposure. Additionally, it is acknowledged for its environmental risks, necessitating proper disposal in accordance with regulatory guidelines.

34662-29-8

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34662-29-8 Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-4-nitrobenzonitrile is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to serve as a building block for the development of organic compounds that address specific medical needs.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Chloro-4-nitrobenzonitrile is employed as an intermediate for the production of agrochemicals. Its properties contribute to the creation of compounds that can be used in pest control and crop protection, thereby supporting agricultural productivity.
Used in Dye Industry:
3-Chloro-4-nitrobenzonitrile is also used as an intermediate in the dye industry. Its chemical structure is leveraged to produce dyes that are used in various applications, including textiles, plastics, and printing inks, to impart color and enhance visual appeal.
Used in Industrial Applications:
Beyond its role in specific industries, 3-Chloro-4-nitrobenzonitrile is recognized for its broader applications in various industrial processes. Its versatility as a building block for organic compounds makes it valuable for a range of uses, from chemical manufacturing to the development of new materials with specific properties.

Check Digit Verification of cas no

The CAS Registry Mumber 34662-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,6 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34662-29:
(7*3)+(6*4)+(5*6)+(4*6)+(3*2)+(2*2)+(1*9)=118
118 % 10 = 8
So 34662-29-8 is a valid CAS Registry Number.

34662-29-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-4-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names 3-chloro-4-nitro-benzonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34662-29-8 SDS

34662-29-8Relevant academic research and scientific papers

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

-

Page/Page column 22, (2010/11/08)

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

-

, (2008/06/13)

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

Benzimidazole and pyridylimidazole derivatives

-

, (2008/06/13)

This invention relates to benzimidazoles, pyridylimidazoles and related bicyclic heteroaryl compounds, all of which may be described by of Formula I The invention is particularly related to such compounds that bind with high selectivity and high affinity to the benzodiazepine site of GABAA receptors. This invention also relates to pharmaceutical compositions comprising such compounds and to the use of such compounds in treatment of certain central nervous system (CNS) diseases. Novel processes for preparing compounds of Formula I are disclosed. This invention also relates to the use of benzimidazoles, pyridylimidazoles and related bicyclic heteroaryl compounds of Formula I in combination with one or more other CNS agents to potentiate the effects of the other CNS agents. Additionally this invention relates to the use such compounds as probes for the localization of GABAA receptors in tissue sections.

Novel benzotriazoles anti-inflammatory compounds

-

Page 59, (2010/11/29)

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

Studies on antiinflammatory agents. I. Synthesis and pharmacological properties of 2'-phenoxymethanesulfonanilide derivatives

Tsuji,Nakamura,Konishi,Okumura,Matsuo

, p. 2399 - 2409 (2007/10/02)

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.

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