Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate - 59337-92-7

Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate

Catalog Number: EVT-327710
CAS Number: 59337-92-7
Molecular Formula: C6H5ClO4S2
Molecular Weight: 240.7 g/mol
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Product Introduction

Description
Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate is a chemical compound that belongs to the class of thiophene derivatives. It is a synthetic compound that has gained significant attention in the scientific community due to its potential biological and industrial applications.
Applications in Various Fields
Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate has potential applications in medical, environmental, and industrial research. In medical research, the compound can be used in drug development to treat various diseases, including cancer, bacterial and fungal infections, and inflammation. The compound has shown promising results in preclinical studies, and clinical trials are underway to determine its safety and efficacy in humans. In environmental research, the compound can be used to study its effects on ecosystems and its role in pollution management. The compound can also be used in industrial research to improve product quality and efficiency. However, the use of the compound in industrial processes can pose health and safety concerns, and proper safety protocols must be followed.

Properties

CAS Number

59337-92-7

Product Name

Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate

IUPAC Name

methyl 3-chlorosulfonylthiophene-2-carboxylate

Molecular Formula

C6H5ClO4S2

Molecular Weight

240.7 g/mol

InChI

InChI=1S/C6H5ClO4S2/c1-11-6(8)5-4(2-3-12-5)13(7,9)10/h2-3H,1H3

InChI Key

PJVJBDAUWILEOG-UHFFFAOYSA-N

SMILES

COC(=O)C1=C(C=CS1)S(=O)(=O)Cl

Canonical SMILES

COC(=O)C1=C(C=CS1)S(=O)(=O)Cl
Method of Synthesis or Extraction
Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate can be synthesized using various methods, including the reaction of 3-thiophenecarboxylic acid with chlorosulfonic acid and methanol. The efficiency and yield of the synthesis process depend on the reaction conditions, such as temperature, pressure, and reaction time. The yield of the synthesis process can be improved by optimizing the reaction conditions. However, the synthesis process requires the use of hazardous chemicals, which can pose environmental and safety concerns. Therefore, it is essential to follow proper safety protocols and dispose of the waste materials appropriately.
Chemical Structure and Biological Activity
Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate has a molecular formula of C7H5ClO4S2 and a molecular weight of 256.7 g/mol. The compound has a thiophene ring with a carboxylate and chlorosulfonyl functional group attached to it. The compound has shown potential biological activity, including antimicrobial, antifungal, and anti-inflammatory properties. The mechanism of action of the compound involves the inhibition of enzymes and proteins involved in the biological processes.
Biological Effects
Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate has shown potential therapeutic effects in various diseases, including cancer, bacterial and fungal infections, and inflammation. The compound has been found to inhibit the growth of cancer cells and reduce inflammation in animal models. However, the compound can also have toxic effects on cells and tissues, leading to adverse health effects. Therefore, it is essential to determine the optimal dose and duration of treatment to minimize the potential toxic effects.
Future Perspectives and Challenges
The use of methyl 3-(chlorosulfonyl)thiophene-2-carboxylate in scientific research is still in its early stages, and there are several challenges associated with its use. One of the major challenges is the potential toxic effects of the compound on cells and tissues. Therefore, it is essential to determine the optimal dose and duration of treatment to minimize the potential toxic effects. Another challenge is the limited availability of the compound, which can hinder its use in scientific research. However, with the development of new synthesis methods and the optimization of existing methods, the availability of the compound can be increased. In the future, the compound has the potential to be used in various fields, including medicine, environmental research, and industrial research, to improve human health and the environment.
Conclusion:
Methyl 3-(chlorosulfonyl)thiophene-2-carboxylate is a synthetic compound that has shown potential biological and industrial applications. The compound can be synthesized using various methods, and its efficiency and yield depend on the reaction conditions. The compound has a thiophene ring with a carboxylate and chlorosulfonyl functional group attached to it and has shown potential biological activity, including antimicrobial, antifungal, and anti-inflammatory properties. The compound has potential therapeutic effects in various diseases, including cancer, bacterial and fungal infections, and inflammation. However, the compound can also have toxic effects on cells and tissues, leading to adverse health effects. Therefore, it is essential to determine the optimal dose and duration of treatment to minimize the potential toxic effects. The compound has potential applications in medical, environmental, and industrial research, and its use can improve human health and the environment.

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