Thiophene-2-thiol
Inhibitors/Agonists
Thiophene-2-thiol is a sulfur-containing heterocyclic compound that has gained significant attention in scientific research due to its diverse biological and industrial applications. It is a colorless liquid with a pungent odor and is commonly used as a precursor in the synthesis of various organic compounds.
116.2 g/mol
116.2 g/mol
Formulation:
116.2 g/mol
Source:
Usage:
Thiophene-2-thiol
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-521770
CAS Number: 7774-74-5
Molecular Formula: C4H4S2
Molecular Weight: 116.2 g/mol
Purity: ≥ 95%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 1g | bt-521770-1g | $296.62 | |
| 5g | bt-521770-5g | $349.23 | |
| 10g | bt-521770-10g | $659.08 | |
| 25g | bt-521770-25g | $1,285.23 | |
| 100g | bt-521770-100g | $4,218.46 | |
| 500g | bt-521770-500g | $17,665.08 |
| CAS Number | 7774-74-5 |
|---|---|
| Product Name | Thiophene-2-thiol |
| Molecular Formula | C4H4S2 |
| Molecular Weight | 116.2 g/mol |
| Density | d204 1.24 1.250-1.255 |
| InChI | InChI=1S/C4H4S2/c5-4-2-1-3-6-4/h1-3,5H |
| InChI Key | SWEDAZLCYJDAGW-UHFFFAOYSA-N |
| IUPAC Name | thiophene-2-thiol |
| Canonical SMILES | C1=CSC(=C1)S |
| Description | Thiophene-2-thiol is a sulfur-containing heterocyclic compound that has gained significant attention in scientific research due to its diverse biological and industrial applications. It is a colorless liquid with a pungent odor and is commonly used as a precursor in the synthesis of various organic compounds. |
| Method of Synthesis or Extraction | Thiophene-2-thiol can be synthesized by various methods, including the reaction of thiophene with hydrogen sulfide, the reaction of thiophene with sodium hydrosulfide, and the reaction of thiophene with sulfur and hydrogen sulfide. The efficiency and yield of each method vary depending on the reaction conditions, such as temperature, pressure, and catalysts used. The environmental and safety considerations associated with the synthesis of thiophene-2-thiol include the release of toxic gases, such as hydrogen sulfide, and the use of hazardous chemicals, such as sulfuric acid. |
| Chemical Structure and Biological Activity | The chemical structure of thiophene-2-thiol consists of a thiophene ring with a sulfur atom attached to it. It has been found to exhibit various biological activities, including antimicrobial, antifungal, and anticancer properties. The mechanism of action and biological targets of thiophene-2-thiol are not fully understood, but it is believed to act by inhibiting enzymes and disrupting cellular processes. |
| Biological Effects | Thiophene-2-thiol has been shown to have both therapeutic and toxic effects on cell function and signal transduction. It has been found to induce apoptosis in cancer cells and inhibit the growth of bacteria and fungi. However, it has also been shown to have toxic effects on normal cells and can cause oxidative stress and DNA damage. The potential therapeutic and toxic effects of thiophene-2-thiol are still being studied. |
| Applications | Thiophene-2-thiol has various applications in medical, environmental, and industrial research. In medical research, it has been studied for its role in drug development and has shown promising results in preclinical studies. It has also been used in clinical trials for the treatment of various diseases, including cancer and fungal infections. In environmental research, it has been studied for its effects on ecosystems and its role in pollution management. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency. However, health and safety considerations must be taken into account when using thiophene-2-thiol in industrial applications. |
| Future Perspectives and Challenges | The current limitations in the use and study of thiophene-2-thiol include its toxicity and the lack of understanding of its mechanism of action. Possible solutions and improvements include the development of safer and more efficient synthesis methods and the identification of its biological targets. Future trends and prospects in the application of thiophene-2-thiol in scientific research include its potential use in the development of new drugs and its role in environmental sustainability. Conclusion: Thiophene-2-thiol is a sulfur-containing heterocyclic compound with diverse biological and industrial applications. Its synthesis methods, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges have been discussed in this paper. Further research is needed to fully understand the potential therapeutic and toxic effects of thiophene-2-thiol and to develop safer and more efficient synthesis methods. |
| Other CAS Number | 7774-74-5 |
| Physical Description | Liquid Oily, colourless to orange liquid; powerful, sulferaceous, burnt-caramel, roasted-coffee odou |
| Pictograms | Irritant |
| SMILES | C1=CSC(=C1)S |
| Solubility | Very slightly soluble in water Miscible at room temperature (in ethanol) |
| Synonyms | 2-Mercaptothiophene; 2-Thienylmercaptan; α-Thienyl Mercaptan |
| PubChem Compound | Thiophene-2-thiol |
| Last Modified | May 29 2023 |