5-Nitrothiophene-2-carbonitrile
Inhibitors/Agonists
5-Nitrothiophene-2-carbonitrile is a heterocyclic organic compound with the molecular formula C5H2N2OS. It is a yellow crystalline solid that is used in various fields such as medical research, environmental research, and industrial research. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of 5-Nitrothiophene-2-carbonitrile.
154.15 g/mol
154.15 g/mol
Formulation:
154.15 g/mol
Source:
Usage:
5-Nitrothiophene-2-carbonitrile
The product is for non-human research only. Not for therapeutic or veterinary use.
Catalog Number: BT-319293
CAS Number: 16689-02-4
Molecular Formula: C5H2N2O2S
Molecular Weight: 154.15 g/mol
Purity: ≥ 97%
Inventory: In Stock
| Size | SKU | Price | |
|---|---|---|---|
| 1g | bt-319293-1g | $295.85 | |
| 5g | bt-319293-5g | $841.38 | |
| 10g | bt-319293-10g | $1,617.23 | |
| 25g | bt-319293-25g | $3,029.38 | |
| 100g | bt-319293-100g | $10,144.15 |
| CAS Number | 16689-02-4 |
|---|---|
| Product Name | 5-Nitrothiophene-2-carbonitrile |
| Molecular Formula | C5H2N2O2S |
| Molecular Weight | 154.15 g/mol |
| InChI | InChI=1S/C5H2N2O2S/c6-3-4-1-2-5(10-4)7(8)9/h1-2H |
| InChI Key | FLYONFCGDKAMIH-UHFFFAOYSA-N |
| IUPAC Name | 5-nitrothiophene-2-carbonitrile |
| Canonical SMILES | C1=C(SC(=C1)[N+](=O)[O-])C#N |
| Description | 5-Nitrothiophene-2-carbonitrile is a heterocyclic organic compound with the molecular formula C5H2N2OS. It is a yellow crystalline solid that is used in various fields such as medical research, environmental research, and industrial research. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges of 5-Nitrothiophene-2-carbonitrile. |
| Method of Synthesis or Extraction | There are several methods for synthesizing 5-Nitrothiophene-2-carbonitrile, including the reaction of 2-thiophenecarbonitrile with nitric acid, the reaction of 2-thiophenecarbonitrile with nitrous acid, and the reaction of 2-thiophenecarbonitrile with nitric oxide. The efficiency and yield of each method vary depending on the reaction conditions. For example, the reaction of 2-thiophenecarbonitrile with nitric acid yields 5-Nitrothiophene-2-carbonitrile with a yield of 70-80%. However, this method requires the use of concentrated nitric acid, which is highly corrosive and can cause severe burns. Therefore, safety precautions must be taken when using this method. |
| Chemical Structure and Biological Activity | The chemical structure of 5-Nitrothiophene-2-carbonitrile consists of a thiophene ring with a nitro group and a cyano group attached to it. The compound has been found to exhibit various biological activities, including antimicrobial, antifungal, and anticancer activities. The mechanism of action of 5-Nitrothiophene-2-carbonitrile involves the inhibition of enzymes and proteins involved in cell growth and proliferation. |
| Biological Effects | Studies have shown that 5-Nitrothiophene-2-carbonitrile can affect cell function and signal transduction pathways. It has been found to induce apoptosis in cancer cells and inhibit the growth of various microorganisms. However, the compound can also have potential toxic effects on cells and organisms, and its use must be carefully monitored. |
| Applications | In medical research, 5-Nitrothiophene-2-carbonitrile has been studied for its potential role in drug development. It has been found to exhibit promising anticancer activity and is being investigated as a potential treatment for various types of cancer. In environmental research, the compound has been studied for its effects on ecosystems and its potential role in pollution management. In industrial research, 5-Nitrothiophene-2-carbonitrile is used in manufacturing processes to improve product quality and efficiency. However, health and safety considerations must be taken into account when using the compound in industrial settings. |
| Future Perspectives and Challenges | Despite the promising biological activities of 5-Nitrothiophene-2-carbonitrile, there are still limitations in its use and study. For example, the compound can have potential toxic effects on cells and organisms, and its use must be carefully monitored. Future research should focus on developing safer and more efficient methods for synthesizing and using the compound. Additionally, further studies are needed to fully understand the biological effects and potential therapeutic applications of 5-Nitrothiophene-2-carbonitrile. |
| Pictograms | Corrosive;Acute Toxic;Irritant |
| SMILES | C1=C(SC(=C1)[N+](=O)[O-])C#N |
| PubChem Compound | 5-Nitrothiophene-2-carbonitrile |
| Last Modified | May 29 2023 |