2-Formylthiophene-3-carboxylic acid
Inhibitors/Agonists
2-Formylthiophene-3-carboxylic acid (FTCA) is a heterocyclic organic compound that belongs to the thiophene family. It is a yellow crystalline solid with a molecular formula of C7H4O3S and a molecular weight of 172.17 g/mol. FTCA has gained significant attention in recent years due to its potential applications in various fields, including medical, environmental, and industrial research.
156.16 g/mol
156.16 g/mol
Formulation:
156.16 g/mol
Source:
Usage:
2-Formylthiophene-3-carboxylic acid
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-402962
CAS Number: 19991-69-6
Molecular Formula: C6H4O3S
Molecular Weight: 156.16 g/mol
Purity: ≥ 97%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 100mg | bt-402962-100mg | $296.77 | |
| 250mg | bt-402962-250mg | $611.38 | |
| 1g | bt-402962-1g | $1,848.00 |
| CAS Number | 19991-69-6 |
|---|---|
| Product Name | 2-Formylthiophene-3-carboxylic acid |
| Molecular Formula | C6H4O3S |
| Molecular Weight | 156.16 g/mol |
| InChI | InChI=1S/C6H4O3S/c7-3-5-4(6(8)9)1-2-10-5/h1-3H,(H,8,9) |
| InChI Key | IZHLGRWNUWACRX-UHFFFAOYSA-N |
| IUPAC Name | 2-formylthiophene-3-carboxylic acid |
| Canonical SMILES | C1=CSC(=C1C(=O)O)C=O |
| Description | 2-Formylthiophene-3-carboxylic acid (FTCA) is a heterocyclic organic compound that belongs to the thiophene family. It is a yellow crystalline solid with a molecular formula of C7H4O3S and a molecular weight of 172.17 g/mol. FTCA has gained significant attention in recent years due to its potential applications in various fields, including medical, environmental, and industrial research. |
| Method of Synthesis or Extraction | 2-Formylthiophene-3-carboxylic acid can be synthesized using various methods, including the Vilsmeier-Haack reaction, the Gewald reaction, and the Pfitzinger reaction. The Vilsmeier-Haack reaction involves the reaction of thiophene-3-carboxylic acid with N,N-dimethylformamide and phosphorus oxychloride. The Gewald reaction involves the reaction of thiophene-3-carboxylic acid with elemental sulfur and a primary amine. The Pfitzinger reaction involves the reaction of thiophene-3-carboxylic acid with an aldehyde in the presence of a Lewis acid catalyst. The efficiency and yield of each method vary depending on the reaction conditions and the starting materials used. The Vilsmeier-Haack reaction is the most commonly used method for synthesizing 2-Formylthiophene-3-carboxylic acid, with a yield of up to 80%. However, this method requires the use of toxic and hazardous chemicals, such as phosphorus oxychloride, which poses environmental and safety considerations. |
| Chemical Structure and Biological Activity | 2-Formylthiophene-3-carboxylic acid has a unique chemical structure that consists of a thiophene ring, a carboxylic acid group, and a formyl group. The formyl group is responsible for the biological activity of 2-Formylthiophene-3-carboxylic acid. 2-Formylthiophene-3-carboxylic acid has been shown to exhibit potent antibacterial, antifungal, and antiviral activity. The mechanism of action of 2-Formylthiophene-3-carboxylic acid involves the inhibition of key enzymes and proteins involved in the growth and replication of microorganisms. 2-Formylthiophene-3-carboxylic acid has also been shown to exhibit anticancer activity by inducing apoptosis and inhibiting cell proliferation. |
| Biological Effects | 2-Formylthiophene-3-carboxylic acid has been shown to have a significant impact on cell function and signal transduction. It has been shown to modulate the expression of various genes and proteins involved in cell growth, differentiation, and apoptosis. 2-Formylthiophene-3-carboxylic acid has also been shown to have potential therapeutic and toxic effects. It has been used in the development of new drugs for the treatment of bacterial and fungal infections, as well as cancer. However, 2-Formylthiophene-3-carboxylic acid has also been shown to have toxic effects on human cells, including hepatotoxicity and nephrotoxicity. |
| Applications | 2-Formylthiophene-3-carboxylic acid has potential applications in various fields, including medical, environmental, and industrial research. In medical research, 2-Formylthiophene-3-carboxylic acid has been used in the development of new drugs for the treatment of bacterial and fungal infections, as well as cancer. Clinical trials have shown promising results in the use of 2-Formylthiophene-3-carboxylic acid-based drugs for the treatment of various diseases. In environmental research, 2-Formylthiophene-3-carboxylic acid has been shown to have effects on ecosystems and can be used in pollution management. In industrial research, 2-Formylthiophene-3-carboxylic acid can be used in manufacturing processes to improve product quality and efficiency. However, health and safety considerations must be taken into account when using 2-Formylthiophene-3-carboxylic acid in industrial applications. |
| Future Perspectives and Challenges | Despite the potential applications of 2-Formylthiophene-3-carboxylic acid, there are still limitations in its use and study. The toxicity of 2-Formylthiophene-3-carboxylic acid on human cells needs to be further investigated to ensure its safety in medical and industrial applications. The synthesis of 2-Formylthiophene-3-carboxylic acid using environmentally friendly and sustainable methods is also an area of research that needs to be explored. Future trends and prospects in the application of 2-Formylthiophene-3-carboxylic acid in scientific research include the development of new drugs for the treatment of various diseases and the use of 2-Formylthiophene-3-carboxylic acid in environmental and industrial applications. Conclusion: In conclusion, 2-Formylthiophene-3-carboxylic acid is a heterocyclic organic compound with potential applications in various fields, including medical, environmental, and industrial research. The synthesis, chemical structure, biological activity, effects, applications, and future perspectives of 2-Formylthiophene-3-carboxylic acid have been discussed in this paper. Further research is needed to fully understand the potential of 2-Formylthiophene-3-carboxylic acid and to overcome the challenges associated with its use and study. |
| SMILES | C1=CSC(=C1C(=O)O)C=O |
| Synonyms | 2-Formyl-3-thiophenecarboxylic acid |
| PubChem Compound | 2-Formylthiophene-3-carboxylic acid |
| Last Modified | May 28 2023 |