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5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chloride is a chemical compound that serves as a versatile building block in organic synthesis and pharmaceutical research. It is characterized by the presence of a sulfonyl chloride group attached to a substituted benzene ring, which allows for the formation of various carbon-sulfur and carbon-oxygen bonds. 5-BroMo-4-chloro-2-fluoro-benzenesulfonylchloride is known for its reactivity and stability, making it an essential component in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.

1070972-67-6

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1070972-67-6 Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chloride is used as a reagent for the introduction of sulfonyl chloride groups in various organic molecules, which is crucial for the synthesis of pharmaceutical compounds. Its ability to form carbon-sulfur and carbon-oxygen bonds makes it a valuable intermediate in the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chloride is utilized in the synthesis of sulfonyl fluorides, which are important intermediates for the production of agrochemicals. These sulfonyl fluorides contribute to the development of effective pesticides and herbicides, enhancing crop protection and yield.
Used in Fine Chemical Industry:
5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chloride is also employed in the fine chemical industry for the synthesis of various specialty chemicals. Its versatility in forming different types of chemical bonds allows for the creation of unique and complex molecules with specific applications in various fields, such as materials science, fragrances, and dyes.
Overall, 5-Bromo-4-chloro-2-fluoro-benzenesulfonyl chloride is a valuable chemical reagent with a wide range of applications in the pharmaceutical, agrochemical, and fine chemical industries. Its ability to introduce sulfonyl chloride groups and form carbon-sulfur and carbon-oxygen bonds makes it an essential component in the development of new and innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 1070972-67-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,9,7 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1070972-67:
(9*1)+(8*0)+(7*7)+(6*0)+(5*9)+(4*7)+(3*2)+(2*6)+(1*7)=156
156 % 10 = 6
So 1070972-67-6 is a valid CAS Registry Number.

1070972-67-6SDS

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 5-bromo-4-chloro-2-fluorobenzenesulfonyl chloride

1.2 Other means of identification

Product number -
Other names 5-Bromo-4-chloro-2-fluorobenzenesulfonylchloride

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:1070972-67-6 SDS

1070972-67-6Downstream Products

1070972-67-6Relevant academic research and scientific papers

GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS AND METHODS RELATING THERETO

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Page/Page column 46; 72-73, (2008/12/04)

GnRH receptor antagonists are disclosed which have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R1a, R1b, R1c, R1d, R2, R2a, and A are as defined herein, including stereoisomers, esters, solvates, and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.

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