3-Methylthiophene-2-carboxylic acid
Catalog Number: BT-256981
CAS Number: 23806-24-8
Molecular Formula: C6H6O2S
Molecular Weight: 142.18 g/mol
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Product Introduction
Description
3-Methylthiophene-2-carboxylic acid is a heterocyclic organic compound that belongs to the thiophene family. It is a yellow crystalline solid that is soluble in organic solvents. This compound has gained significant attention in the scientific community due to its potential biological and industrial applications.
Properties
CAS Number
23806-24-8
Product Name
3-Methylthiophene-2-carboxylic acid
IUPAC Name
3-methylthiophene-2-carboxylic acid
Molecular Formula
C6H6O2S
Molecular Weight
142.18 g/mol
InChI
InChI=1S/C6H6O2S/c1-4-2-3-9-5(4)6(7)8/h2-3H,1H3,(H,7,8)
InChI Key
IFLKEBSJTZGCJG-UHFFFAOYSA-N
SMILES
CC1=C(SC=C1)C(=O)O
Solubility
Soluble in DMSO
Synonyms
AC30341; AC-30341; AC 30341;
Canonical SMILES
CC1=C(SC=C1)C(=O)O
Method of Synthesis or Extraction
There are several methods for synthesizing 3-Methylthiophene-2-carboxylic acid, including the reaction of 3-methylthiophene with carbon dioxide and a base, the reaction of 3-methylthiophene with carbon monoxide and a palladium catalyst, and the reaction of 3-methylthiophene with carbon disulfide and a base. The efficiency and yield of each method vary depending on the reaction conditions. The reaction of 3-methylthiophene with carbon dioxide and a base has been reported to yield up to 80% of the desired product. However, this method requires high pressure and temperature, which can be hazardous. The reaction of 3-methylthiophene with carbon monoxide and a palladium catalyst has been reported to yield up to 90% of the desired product. This method is more efficient and safer than the previous method. The reaction of 3-methylthiophene with carbon disulfide and a base has been reported to yield up to 70% of the desired product. This method is less efficient than the previous two methods but is safer and more environmentally friendly.
Chemical Structure and Biological Activity
The chemical structure of 3-Methylthiophene-2-carboxylic acid consists of a thiophene ring with a carboxylic acid group and a methyl group attached to it. This compound has been reported to exhibit various biological activities, including antimicrobial, antifungal, and anticancer activities. The mechanism of action and biological targets of 3-Methylthiophene-2-carboxylic acid are not fully understood. However, it has been suggested that this compound may act by inhibiting enzymes or interfering with cell signaling pathways.
Biological Effects
Studies have shown that 3-Methylthiophene-2-carboxylic acid can affect cell function and signal transduction. It has been reported to inhibit the growth of various microorganisms, including bacteria and fungi. This compound has also been shown to induce apoptosis in cancer cells. However, the potential therapeutic and toxic effects of 3-Methylthiophene-2-carboxylic acid are not fully understood and require further investigation.
Applications
In medical research, 3-Methylthiophene-2-carboxylic acid has been studied for its potential role in drug development. It has been reported to exhibit anticancer activity and may be useful in the development of new cancer therapies. Clinical trials are needed to determine the safety and efficacy of this compound in humans. In environmental research, 3-Methylthiophene-2-carboxylic acid has been studied for its effects on ecosystems and its role in pollution management. This compound may be useful in the treatment of contaminated soil and water. In industrial research, 3-Methylthiophene-2-carboxylic acid has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations are important when using this compound in industrial settings.
Future Perspectives and Challenges
The current limitations in the use and study of 3-Methylthiophene-2-carboxylic acid include the lack of understanding of its mechanism of action and biological targets. Possible solutions and improvements include further research to elucidate the biological effects of this compound and the development of new synthetic methods to improve efficiency and yield. Future trends and prospects in the application of 3-Methylthiophene-2-carboxylic acid in scientific research include the development of new drugs and therapies for various diseases and the use of this compound in environmental and industrial applications.
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