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What is 2-cyclohexylmercapto-acrylonitrile
**Introduction to 2-Cyclohexylmercapto-acrylonitrile** 2-Cyclohexylmercapto-acrylonitrile is a specialized organic compound featuring a cyclohexylthio group attached to an acrylonitrile backbone. This versatile chemical serves as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, combining a reactive nitrile group with a sulfur-containing cyclohexyl moiety, enables applications in nucleophilic addition reactions and polymer modifications. The compound's stability and reactivity make it valuable for developing bioactive molecules and functionalized polymers. With its potential in fine chemical manufacturing, 2-cyclohexylmercapto-acrylonitrile is an important building block for researchers and industries focused on innovative chemical solutions. Proper handling and storage are essential due to its reactive nature. (Word count: 100)
Preparation Process: To prepare **2-cyclohexylmercapto-acrylonitrile**, follow these steps: 1. **React acrylonitrile (CH₂=CH-CN) with cyclohexyl mercaptan (C₆H₁₁SH)** in the presence of a base (e.g., NaOH or KOH) in an inert solvent (e.g., ethanol or THF) at room temperature. 2. The thiol group (–SH) of cyclohexyl mercaptan adds to the β-carbon of acrylonitrile via a **Michael addition**, forming the desired product. 3. Stir the mixture for 4–6 hours, then quench with water. 4. Extract the product with an organic solvent (e.g., ethyl acetate), dry (Na₂SO₄), and concentrate under reduced pressure. 5. Purify by column chromatography if necessary.
Usage Scenarios: 2-Cyclohexylmercapto-acrylonitrile is primarily used as a chemical intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and specialty polymers. Its acrylonitrile moiety enables participation in polymerization reactions, while the cyclohexylmercapto group enhances solubility and reactivity in various organic transformations. The compound is valuable in Michael addition reactions, serving as a building block for sulfur-containing heterocycles and functionalized nitriles. It may also act as a precursor for corrosion inhibitors or stabilizers in industrial applications. Additionally, its unique structure makes it useful in material science for modifying polymer properties, such as thermal stability and mechanical strength. Research applications include studying thiol-ene click chemistry and radical-mediated processes.
2-cyclohexylmercapto-acrylonitrile Basic Info
2-cyclohexylmercapto-acrylonitrile Price
1. United States: $100–$300 per kg
2. China: $80–$250 per kg
3. Russia: No results
4. Germany: $120–$350 per kg
5. India: $90–$280 per kg
6. Japan: $150–$400 per kg
7. Brazil: No results
8. South Korea: $130–$320 per kg
9. Philippines: No results
10. United Kingdom: $140–$360 per kg
11. France: $130–$340 per kg
12. Mexico: No results
13. Canada: $110–$330 per kg
14. South Africa: No results
15. Egypt: No results
16. Turkey: No results
17. Thailand: No results
18. Indonesia: No results
These ranges are approximate and based on general market trends for specialty chemicals. Prices may vary significantly depending on supplier, purity, and quantity. If no results are listed, it indicates that pricing data is unavailable or the product is not commonly traded in that market.
Synthesis Route
Total1 synthetic routes
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