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Methyl 3-chlorosulfonylthiophene-2-carboxylate CAS:59337-92-7

Methyl 3-chlorosulfonylthiophene-2-carboxylate is a chemical compound featuring a thiophene ring substituted with a chlorosulfonyl group and a methyl ester at the carboxylic acid position. With the molecular formula C7H6ClO3S, this compound exhibits significant reactivity due to the presence of the sulfonyl and chlorine functional groups. It has attracted attention in organic synthesis and materials science for its potential applications in developing biologically active molecules.


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Application and Effect:

Methyl 3-chlorosulfonylthiophene-2-carboxylate serves multiple roles in organic chemistry, particularly as an intermediate in the synthesis of various bioactive compounds. The presence of the chlorosulfonyl group enhances its reactivity, making it a valuable building block for constructing more complex structures through nucleophilic substitution reactions. This functionality enables the introduction of diverse substituents, allowing chemists to tailor the final products for specific biological activities. In pharmaceutical research, derivatives synthesized from methyl 3-chlorosulfonylthiophene-2-carboxylate have shown promise for potential therapeutic applications. The thiophene ring, known for its ability to modulate various biological pathways, may impart desirable pharmacological properties to the resulting compounds. Researchers are exploring its potential as a candidate for developing new drugs targeting inflammation, cancer, or infectious diseases. By modifying the structure of this compound, scientists aim to enhance activity while minimizing side effects, contributing to innovative treatment strategies. Additionally, this compound finds utility in the agrochemical sector, where it can be transformed into herbicides or fungicides. The chlorosulfonyl group provides unique reactivity that can be exploited to design selective agents for crop protection. By creating formulations based on methyl 3-chlorosulfonylthiophene-2-carboxylate, researchers can develop effective solutions to combat agricultural pests and diseases, promoting sustainable farming practices. Furthermore, in materials science, methyl 3-chlorosulfonylthiophene-2-carboxylate can participate in polymerization reactions to generate functionalized polymers with tailored properties. These materials may exhibit enhanced thermal stability, conductivity, or other characteristics beneficial for use in electronics or coatings. Overall, methyl 3-chlorosulfonylthiophene-2-carboxylate represents a versatile compound with significant potential in drug development, agrochemistry, and materials science. Its ability to serve as a reactive intermediate underscores its importance in advancing chemical synthesis and innovation across various scientific fields.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C7H6ClO3S
Assay 99%
Appearance white powder
CAS No.  59337-92-7
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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