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2,1,3-Benzothiadiazole-4-sulfonyl chloride, with the molecular formula C7H4ClNOS2, is a sulfonyl chloride derivative of benzothiadiazole. It is a key building block in the synthesis of a variety of organic compounds, characterized by its versatile chemical structure that allows for modification and functionalization. 2,1,3-BENZOTHIADIAZOLE-4-SULFONYL CHLORIDE is recognized as an important reagent in organic synthesis, particularly for its ability to introduce the benzothiadiazole-4-sulfonyl group into various molecules, facilitating the creation of diverse and complex chemical structures.

73713-79-8

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73713-79-8 Usage

Uses

Used in Pharmaceutical Industry:
2,1,3-Benzothiadiazole-4-sulfonyl chloride is used as a key intermediate for the production of pharmaceuticals. Its incorporation into drug molecules can enhance their therapeutic properties and pharmacological activities, contributing to the development of new and improved medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,1,3-Benzothiadiazole-4-sulfonyl chloride serves as an essential intermediate in the synthesis of various agrochemicals. Its use in this industry aids in the development of effective pesticides, herbicides, and other agricultural chemicals that are crucial for crop protection and yield enhancement.
Used in Materials Science:
2,1,3-Benzothiadiazole-4-sulfonyl chloride is used as a precursor in the synthesis of conducting polymers and dyes. Its unique properties enable the creation of materials with specific electrical, optical, and color characteristics, which are valuable in various applications, including electronic devices, sensors, and colorants for different industries.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2,1,3-Benzothiadiazole-4-sulfonyl chloride is used to introduce the benzothiadiazole-4-sulfonyl group into target molecules. This allows for the functionalization of organic compounds, leading to the formation of new chemical entities with potential applications in various fields, such as medicinal chemistry, material science, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 73713-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,1 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73713-79:
(7*7)+(6*3)+(5*7)+(4*1)+(3*3)+(2*7)+(1*9)=138
138 % 10 = 8
So 73713-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClN2O2S2/c7-13(10,11)5-3-1-2-4-6(5)9-12-8-4/h1-3H

73713-79-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H50377)  2,1,3-Benzothiadiazole-4-sulfonyl chloride, 97%   

  • 73713-79-8

  • 1g

  • 2223.0CNY

  • Detail
  • Alfa Aesar

  • (H50377)  2,1,3-Benzothiadiazole-4-sulfonyl chloride, 97%   

  • 73713-79-8

  • 5g

  • 10017.0CNY

  • Detail

73713-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,1,3-BENZOTHIADIAZOLE-4-SULFONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names 4-Chlorosulfonyl-2,1,3-benzothiadiazole

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:73713-79-8 SDS

73713-79-8Relevant academic research and scientific papers

A convenient synthesis of novel 3-(heterocyclylsulfonyl)propanoic acids and their amide derivatives

Dorogov, Mikhail V.,Filimonov, Sergey I.,Kobylinsky, Dmitry B.,Ivanovsky, Sergey A.,Korikov, Pavel V.,Soloviev, Mikhail Y.,Khahina, Maria Y.,Shalygina, Elena E.,Kravchenko, Dmitry V.,Ivachtchenko, Alexandre V.

, p. 2999 - 3004 (2007/10/03)

A large number of novel 3-(heterocyclylsulfonyl)propanoic acids and their amide derivatives were prepared in good yields and excellent purity starting from the corresponding heterocyclic compounds. At first, chlorosulfonates were generated by reaction of initial heterocycles with various sulfonating and chlorinating agents followed by their conversion into sodium sulfinates. Treatment of sulfinates with acrylic acid smoothly afforded a series of sulfonylpropionates, which were used as convenient reagents for the preparation of a large number of the corresponding carboxamide derivatives.

DISULFIDES OF THE BENZO-2,1,3-THIADIAZOLE SERIES

Belen'kaya, I. A.,Shulla, T. A.

, p. 1303 - 1307 (2007/10/02)

Disulfides of the benzo-2,1,3-thiadiazole series were obtained by reduction of benzo-2,1,3-thiadiazolesulfonyl chlorides (by hydriodic acid or by sulfur dioxide) or by the reaction of benzo-2,1,3-thiadiazolesulfinic acids with hydrogen bromide in acetic acid.Convenient methods for the synthesis of the starting compounds were found, and the fungicidal activity of the disulfides obtained was studied.

Herbicidal sulfonamides

-

, (2008/06/13)

This invention relates to novel sulfonylurea herbicidal compounds, agriculturally suitable compositions thereof and a method-of-use of said compounds and compositions as general preemergence and/or postemergence herbicides or their use as plant growth regulants.

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