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2-Thiophenecarboxylic acid, 3,4-dichloro-, is a chemical compound with the molecular formula C6H3Cl2O2S. It is a derivative of thiophene carboxylic acid, featuring two chlorine atoms attached to the 3 and 4 positions of the aromatic ring. 2-Thiophenecarboxylic acid, 3,4-dichlorois recognized for its potential applications in various fields, including organic chemistry, pharmaceuticals, agrochemicals, and materials science, due to its unique structural properties and reactivity.

61209-02-7

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61209-02-7 Usage

Uses

Used in Pharmaceutical Industry:
2-Thiophenecarboxylic acid, 3,4-dichlorois used as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Thiophenecarboxylic acid, 3,4-dichloroserves as a precursor for the synthesis of various agrochemicals, including pesticides and herbicides. Its ability to chelate metal ions and form coordination complexes enhances its utility in this field.
Used in Materials Science:
2-Thiophenecarboxylic acid, 3,4-dichlorois utilized as a building block in the synthesis of advanced materials with specific properties, such as conductivity, stability, and reactivity. Its incorporation into these materials can lead to the development of new technologies and applications.
Used in Organic Chemistry:
As a versatile organic compound, 2-Thiophenecarboxylic acid, 3,4-dichlorois employed in various organic synthesis processes. Its reactivity and functional groups make it a valuable component in the preparation of complex organic molecules and compounds.
Used in Anticancer and Antimicrobial Applications:
2-Thiophenecarboxylic acid, 3,4-dichloroexhibits potential anticancer and antimicrobial activities. It can be used as a therapeutic agent or incorporated into drug formulations to target and treat various types of cancer and microbial infections.
Used in Coordination Chemistry:
Due to its ability to chelate metal ions, 2-Thiophenecarboxylic acid, 3,4-dichlorois a versatile building block for the preparation of various coordination complexes in coordination chemistry. These complexes can have diverse applications, such as catalysts, sensors, and materials with unique properties.

Check Digit Verification of cas no

The CAS Registry Mumber 61209-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,0 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61209-02:
(7*6)+(6*1)+(5*2)+(4*0)+(3*9)+(2*0)+(1*2)=87
87 % 10 = 7
So 61209-02-7 is a valid CAS Registry Number.

61209-02-7SDS

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 3,4-dichlorothiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Thiophenecarboxylic acid,3,4-dichloro

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:61209-02-7 SDS

61209-02-7Upstream product

61209-02-7Downstream Products

61209-02-7Relevant academic research and scientific papers

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