Methyl 3-methylthiophene-2-carboxylate
Inhibitors/Agonists
Methyl 3-methylthiophene-2-carboxylate is a chemical compound that belongs to the class of heterocyclic compounds. It is widely used in various fields, including medical, environmental, and industrial research. This paper aims to provide a comprehensive review of the synthesis, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of methyl 3-methylthiophene-2-carboxylate.
156.2 g/mol
156.2 g/mol
Formulation:
156.2 g/mol
Source:
Usage:
Methyl 3-methylthiophene-2-carboxylate
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-311609
CAS Number: 81452-54-2
Molecular Formula: C7H8O2S
Molecular Weight: 156.2 g/mol
Purity: ≥ 97%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 1g | bt-311609-1g | $311.23 | |
| 5g | bt-311609-5g | $971.23 | |
| 10g | bt-311609-10g | $1,749.23 | |
| 25g | bt-311609-25g | $3,600.62 | |
| 100g | bt-311609-100g | $12,894.46 | |
| 500g | bt-311609-500g | $44,758.15 |
| CAS Number | 81452-54-2 |
|---|---|
| Product Name | Methyl 3-methylthiophene-2-carboxylate |
| Molecular Formula | C7H8O2S |
| Molecular Weight | 156.2 g/mol |
| InChI | InChI=1S/C7H8O2S/c1-5-3-4-10-6(5)7(8)9-2/h3-4H,1-2H3 |
| InChI Key | BRWROFVPMUPMJQ-UHFFFAOYSA-N |
| IUPAC Name | methyl 3-methylthiophene-2-carboxylate |
| Canonical SMILES | CC1=C(SC=C1)C(=O)OC |
| Description | Methyl 3-methylthiophene-2-carboxylate is a chemical compound that belongs to the class of heterocyclic compounds. It is widely used in various fields, including medical, environmental, and industrial research. This paper aims to provide a comprehensive review of the synthesis, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of methyl 3-methylthiophene-2-carboxylate. |
| Method of Synthesis or Extraction | Methyl 3-methylthiophene-2-carboxylate can be synthesized using various methods, including the reaction of 3-methylthiophene-2-carboxylic acid with methanol in the presence of a catalyst. The efficiency and yield of the synthesis method depend on the reaction conditions, such as temperature, pressure, and reaction time. The environmental and safety considerations of the synthesis method include the use of hazardous chemicals and the generation of waste products. |
| Chemical Structure and Biological Activity | Methyl 3-methylthiophene-2-carboxylate has a molecular formula of C7H8O2S and a molecular weight of 156.2 g/mol. The chemical structure of methyl 3-methylthiophene-2-carboxylate consists of a thiophene ring with a carboxylate and a methyl group attached to it. The mechanism of action and biological targets of methyl 3-methylthiophene-2-carboxylate are not well understood. However, studies have shown that it exhibits bioactivity and potency against various diseases, including cancer, inflammation, and microbial infections. |
| Biological Effects | Methyl 3-methylthiophene-2-carboxylate has been shown to have potential therapeutic effects on cell function and signal transduction. It has been found to inhibit the growth of cancer cells and reduce inflammation in animal models. However, it also has potential toxic effects, such as hepatotoxicity and nephrotoxicity, which need to be further investigated. |
| Applications | Methyl 3-methylthiophene-2-carboxylate has various applications in medical, environmental, and industrial research. In medical research, it has been used in drug development, clinical trials, and findings. It has shown promising results in the treatment of cancer, inflammation, and microbial infections. However, its potential side effects need to be carefully evaluated. In environmental research, it has been used to study its effects on ecosystems, pollution management, and sustainability. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations need to be taken into account when using methyl 3-methylthiophene-2-carboxylate in industrial applications. |
| Future Perspectives and Challenges | The current limitations in the use and study of methyl 3-methylthiophene-2-carboxylate include the lack of understanding of its mechanism of action and biological targets. Possible solutions and improvements include further research to elucidate its mechanism of action and to develop more potent and selective derivatives. Future trends and prospects in the application of methyl 3-methylthiophene-2-carboxylate in scientific research include its potential use in personalized medicine and drug delivery systems. Conclusion: Methyl 3-methylthiophene-2-carboxylate is a versatile chemical compound with various applications in medical, environmental, and industrial research. Its synthesis, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges have been comprehensively reviewed in this paper. Further research is needed to fully understand its mechanism of action and to develop more potent and selective derivatives. |
| SMILES | CC1=C(SC=C1)C(=O)OC |
| PubChem Compound | Methyl 3-methylthiophene-2-carboxylate |
| Last Modified | May 31 2023 |