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5-(4-CHLOROBENZAMIDOMETHYL)THIOPHENE-2-SULPHONYL CHLORIDE is a sulfonyl chloride derivative of thiophene, characterized by the presence of a chlorobenzamido group. This chemical compound is known for its enhanced reactivity and versatility in various chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

166964-34-7

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166964-34-7 Usage

Uses

Used in Pharmaceutical Industry:
5-(4-CHLOROBENZAMIDOMETHYL)THIOPHENE-2-SULPHONYL CHLORIDE is used as a key intermediate in the synthesis of sulfonamide drugs and other biologically active molecules. Its unique chemical properties contribute to the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 5-(4-CHLOROBENZAMIDOMETHYL)THIOPHENE-2-SULPHONYL CHLORIDE serves as a crucial building block for the creation of novel agrochemicals. Its reactivity allows for the synthesis of compounds with improved pesticidal properties, contributing to more effective crop protection strategies.
Used in Material Science:
5-(4-CHLOROBENZAMIDOMETHYL)THIOPHENE-2-SULPHONYL CHLORIDE is utilized in the development of new materials and catalysts. Its unique chemical properties enable the creation of innovative materials with enhanced performance characteristics, such as improved catalytic activity or specific binding affinities.
Used in Organic Synthesis:
As a versatile chemical compound, 5-(4-CHLOROBENZAMIDOMETHYL)THIOPHENE-2-SULPHONYL CHLORIDE is widely employed in organic synthesis for the preparation of a variety of organic compounds. Its reactivity and functional group compatibility make it a valuable tool for chemists in designing and synthesizing complex molecular structures.

Check Digit Verification of cas no

The CAS Registry Mumber 166964-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,9,6 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 166964-34:
(8*1)+(7*6)+(6*6)+(5*9)+(4*6)+(3*4)+(2*3)+(1*4)=177
177 % 10 = 7
So 166964-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H9Cl2NO3S2/c13-9-3-1-8(2-4-9)12(16)15-7-10-5-6-11(19-10)20(14,17)18/h1-6H,7H2,(H,15,16)

166964-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[[(4-chlorobenzoyl)amino]methyl]thiophene-2-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names 5-{[(4-Chlorobenzoyl)amino]methyl}thiophene-2-sulfonyl chloride

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:166964-34-7 SDS

166964-34-7Relevant academic research and scientific papers

Design, synthesis, and biological activity of novel, potent, and selective (benzoylaminomethyl)thiophene sulfonamide inhibitors of c-Jun-N-terminal kinase

Rückle, Thomas,Biamonte, Marco,Grippi-Vallotton, Tania,Arkinstall, Steve,Cambet, Yves,Camps, Montserrat,Chabert, Christian,Church, Dennis J.,Halazy, Serge,Jiang, Xuliang,Martinou, Isabelle,Nichols, Anthony,Sauer, Wolfgang,Gotteland, Jean-Pierre

, p. 6921 - 6934 (2007/10/03)

Several lines of evidence support the hypothesis that c-Jun N-terminal kinases (JNKs) play a critical role in a wide range of disease states including cell death (apoptosis)-related and inflammatory disorders (epilepsy, brain, heart and renal ischemia, ne

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