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3-Bromo-5-chlorobenzonitrile is a chemical compound characterized by the molecular formula C7H3BrClN. It presents as a white to off-white powder, exhibiting solubility in organic solvents while being insoluble in water. 3-Bromo-5-chlorobenzonitrile is recognized for its role as a versatile building block and intermediate in the synthesis of a diverse array of products, including pharmaceuticals, agrochemicals, dyes, pigments, and polymers. Its chemical structure, which incorporates both bromine and chlorine atoms, endows it with unique properties that make it a valuable resource in various industrial applications.

304854-55-5

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304854-55-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-5-chlorobenzonitrile is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of molecules with specific biological activities, making it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-5-chlorobenzonitrile serves as an essential building block in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby supporting agricultural productivity.
Used in Dye and Pigment Industry:
3-Bromo-5-chlorobenzonitrile is utilized as a crucial intermediate in the synthesis of dyes and pigments, which are used in a wide range of applications, including textiles, plastics, and printing inks. Its chemical properties enable the creation of vibrant and stable colorants that meet the demands of various industries.
Used in Polymer Industry:
3-Bromo-5-chlorobenzonitrile also plays a significant role in the polymer industry, where it is used as a monomer or intermediate in the production of polymers with specific properties. The incorporation of 3-bromo-5-chlorobenzonitrile into polymer structures can impart desirable characteristics, such as enhanced stability, durability, or specific functional groups, which can be tailored for various applications.
Used in Medicinal Chemistry Research:
Due to its biological activity, 3-Bromo-5-chlorobenzonitrile holds potential for applications in the field of medicinal chemistry research. It can be used as a starting material or a scaffold for the design and synthesis of novel bioactive compounds, which may lead to the discovery of new therapeutic agents or drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 304854-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,8,5 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 304854-55:
(8*3)+(7*0)+(6*4)+(5*8)+(4*5)+(3*4)+(2*5)+(1*5)=135
135 % 10 = 5
So 304854-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrClN/c8-6-1-5(4-10)2-7(9)3-6/h1-3H

304854-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-5-chlorobenzonitrile

1.2 Other means of identification

Product number -
Other names 3-BroMo-5-chlorobenzonitrile

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:304854-55-5 SDS

304854-55-5Downstream Products

304854-55-5Relevant academic research and scientific papers

Potent mGluR5 antagonists: Pyridyl and thiazolyl-ethynyl-3,5-disubstituted- phenyl series

Alagille, David,Dacosta, Herve,Chen, Yelin,Hemstapat, Kamondanai,Rodriguez, Alice,Baldwin, Ronald M.,Conn, Jeffrey P.,Tamagnan, Gilles D.

, p. 3243 - 3247 (2011)

We report the synthesis of four series of 3,5-disubstituted-phenyl ligands targeting the metabotropic glutamate receptor subtype 5: (2-methylthiazol-4-yl) ethynyl (1a-j,), (6-methylpyridin-2-yl)ethynyl (2a-j), (5-methylpyridin-2-yl) ethynyl (3a-j,), and (pyridin-2-yl)ethynyl (4a-j,). The compounds were evaluated for antagonism of glutamate-mediated mobilization of internal calcium in an mGluR5 in vitro assay. All compounds were found to be full antagonists and exhibited low nanomolar to subnanomolar activity.

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