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2-Chloro-5-methylbenzonitrile, a chemical compound with the molecular formula C8H6ClN, is a clear, colorless to pale yellow liquid characterized by a faint, sweet odor. It is a versatile and important chemical in the pharmaceutical and chemical industry, serving as a key intermediate in the synthesis of various organic compounds.

4387-32-0

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4387-32-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-5-methylbenzonitrile is used as an intermediate for the production of pharmaceuticals, contributing to the development of new drugs and medicines. Its unique chemical structure allows for the synthesis of a wide range of pharmaceutical compounds, enhancing the industry's ability to create innovative and effective treatments.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Chloro-5-methylbenzonitrile is utilized as an intermediate in the synthesis of various agrochemicals, including pesticides and herbicides. Its incorporation into these products helps improve agricultural productivity and crop protection.
Used in Organic Compounds Synthesis:
2-Chloro-5-methylbenzonitrile serves as a building block for the synthesis of a variety of organic compounds, such as dyes, pigments, and perfumes. Its reactive nature allows for the creation of diverse and complex molecules, expanding the range of products available in these industries.
Used in Chemical Industry:
As a versatile chemical, 2-Chloro-5-methylbenzonitrile is employed in the chemical industry for various applications, including the production of other organic compounds and the development of new chemical processes. Its presence in this industry highlights its importance and potential for further innovation.
Due to the reactive nature of 2-Chloro-5-methylbenzonitrile, it is crucial to handle this chemical with care and implement appropriate safety precautions to ensure the safety of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 4387-32-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4387-32:
(6*4)+(5*3)+(4*8)+(3*7)+(2*3)+(1*2)=100
100 % 10 = 0
So 4387-32-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClN/c1-6-2-3-8(9)7(4-6)5-10/h2-4H,1H3

4387-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-5-methylbenzonitrile

1.2 Other means of identification

Product number -
Other names 4-Chlor-3-cyanotoluol

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:4387-32-0 SDS

4387-32-0Relevant articles and documents

Water bridges are essential to neonicotinoids: Insights from synthesis, bioassay and molecular modelling studies

Zhu, Chengchun,Li, Guanglong,Xiao, Keya,Shao, Xusheng,Cheng, Jiagao,Li, Zhong

, p. 255 - 258 (2018/05/23)

Water-bridged H-bonds have been observed in many cases of ligand-receptor recognitions. To explore the roles of water bridges in the binding of neonicotinoids with receptors, twenty-four neonicotinoid compounds with nine fragments, including 1H-1,2,3-tria

Palladium-catalyzed highly selective ortho-halogenation (I, Br, Cl) of arylnitriles via sp2 C-H bond activation using cyano as directing group

Du, Bingnan,Jiang, Xiaoqing,Sun, Peipei

, p. 2786 - 2791 (2013/04/24)

A palladium-catalyzed ortho-halogenation (I, Br, Cl) of arylnitrile is described. The optimal reaction conditions were identified after examining various factors such as catalyst, additive, solvent, and reaction temperature. Using cyano as the directing group, the halogenation reaction gave good to excellent yields. The method is compatible to the arylnitriles with either electron-withdrawing or electron-donating groups. The reaction is available to the substrate in at least gram scale. The present method was successfully applied to the synthesis of the precursors of paucifloral F and isopaucifloral F.

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