2,3-Thiophenedicarboxaldehyde
Inhibitors/Agonists
2,3-Thiophenedicarboxaldehyde is a heterocyclic organic compound that contains a thiophene ring and two aldehyde groups. It is a versatile building block in organic synthesis and has gained significant attention in medicinal, environmental, and industrial research.
140.16 g/mol
140.16 g/mol
Formulation:
140.16 g/mol
Source:
Usage:
2,3-Thiophenedicarboxaldehyde
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-318119
CAS Number: 932-41-2
Molecular Formula: C6H4O2S
Molecular Weight: 140.16 g/mol
Purity: ≥ 98%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 200mg | bt-318119-200mg | $302.92 | |
| 250mg | bt-318119-250mg | $551.23 | |
| 1g | bt-318119-1g | $1,160.15 | |
| 5g | bt-318119-5g | $4,704.31 | |
| 10g | bt-318119-10g | $7,657.85 |
| CAS Number | 932-41-2 |
|---|---|
| Product Name | 2,3-Thiophenedicarboxaldehyde |
| Molecular Formula | C6H4O2S |
| Molecular Weight | 140.16 g/mol |
| InChI | InChI=1S/C6H4O2S/c7-3-5-1-2-9-6(5)4-8/h1-4H |
| InChI Key | WSEJZRIZDQWMKQ-UHFFFAOYSA-N |
| IUPAC Name | thiophene-2,3-dicarbaldehyde |
| Canonical SMILES | C1=CSC(=C1C=O)C=O |
| Description | 2,3-Thiophenedicarboxaldehyde is a heterocyclic organic compound that contains a thiophene ring and two aldehyde groups. It is a versatile building block in organic synthesis and has gained significant attention in medicinal, environmental, and industrial research. |
| Method of Synthesis or Extraction | 2,3-Thiophenedicarboxaldehyde can be synthesized by various methods, including the Vilsmeier-Haack reaction, the Gewald reaction, and the Pfitzinger reaction. The Vilsmeier-Haack reaction involves the reaction of thiophene with formamide and phosphorus oxychloride, followed by hydrolysis. The Gewald reaction involves the reaction of thiophene with α-haloesters and cyanides, followed by hydrolysis. The Pfitzinger reaction involves the reaction of thiophene with aldehydes and α-haloesters, followed by hydrolysis. The efficiency and yield of each method depend on the reaction conditions and the starting materials used. The Vilsmeier-Haack reaction is the most commonly used method for the synthesis of 2,3-Thiophenedicarboxaldehyde, with a yield of up to 80%. However, this method requires the use of toxic and hazardous reagents, such as phosphorus oxychloride, which poses environmental and safety considerations. |
| Chemical Structure and Biological Activity | The chemical structure of 2,3-Thiophenedicarboxaldehyde consists of a thiophene ring and two aldehyde groups. The thiophene ring is a five-membered heterocyclic ring that contains a sulfur atom. The aldehyde groups are reactive functional groups that can undergo various chemical reactions. 2,3-Thiophenedicarboxaldehyde has been reported to exhibit various biological activities, including antimicrobial, antifungal, antitumor, and anti-inflammatory activities. The mechanism of action and biological targets of 2,3-Thiophenedicarboxaldehyde are not well understood, but it is believed to act by inhibiting the growth and proliferation of cancer cells and microorganisms. |
| Biological Effects | 2,3-Thiophenedicarboxaldehyde has been shown to have potential therapeutic effects on cell function and signal transduction. It has been reported to inhibit the growth and proliferation of cancer cells, reduce inflammation, and modulate the immune response. However, it also has potential toxic effects, such as cytotoxicity and genotoxicity, which may limit its use in medical research. In environmental research, 2,3-Thiophenedicarboxaldehyde has been shown to have effects on ecosystems, such as inhibiting the growth of algae and aquatic plants. It may also have a role in pollution management, as it can be used as a sensor for detecting pollutants in the environment. |
| Applications | In medical research, 2,3-Thiophenedicarboxaldehyde has been studied for its role in drug development. It has been reported to have potential as an anticancer agent, anti-inflammatory agent, and immunomodulatory agent. Clinical trials are ongoing to evaluate its safety and efficacy in humans. In environmental research, 2,3-Thiophenedicarboxaldehyde has been used as a sensor for detecting pollutants in the environment. It may also have a role in sustainability and environmental impact, as it can be used to develop eco-friendly products. In industrial research, 2,3-Thiophenedicarboxaldehyde has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations must be taken into account when using 2,3-Thiophenedicarboxaldehyde in industrial applications. |
| Future Perspectives and Challenges | The use and study of 2,3-Thiophenedicarboxaldehyde face several limitations, such as its potential toxicity and limited understanding of its mechanism of action. Possible solutions and improvements include the development of safer and more efficient synthesis methods, the identification of its biological targets and mechanism of action, and the evaluation of its safety and efficacy in humans. Future trends and prospects in the application of 2,3-Thiophenedicarboxaldehyde in scientific research include its potential use as a therapeutic agent for various diseases and its role in developing eco-friendly products. Conclusion: 2,3-Thiophenedicarboxaldehyde is a versatile building block in organic synthesis that has gained significant attention in medicinal, environmental, and industrial research. Its chemical structure, biological activity, biological effects, applications, future perspectives, and challenges have been discussed in this paper. Further research is needed to fully understand its potential as a therapeutic agent and its role in sustainability and environmental impact. |
| Pictograms | Irritant |
| SMILES | C1=CSC(=C1C=O)C=O |
| PubChem Compound | 2,3-Thiophenedicarboxaldehyde |
| Last Modified | May 29 2023 |