2-(2-Nitro-4-(trifluoromethyl)phenyl)acetonitrile
97%
- Product Code: 80919
CAS:
13544-06-4
| Molecular Weight: | 230.14 g./mol | Molecular Formula: | C₉H₅F₃N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 36°C | Boiling Point: | 288.1°C |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the synthesis of various agrochemicals and pharmaceuticals due to its unique structural properties. It serves as a key intermediate in the production of herbicides and pesticides, particularly those targeting broadleaf weeds and pests in agricultural settings. Additionally, its trifluoromethyl group enhances the biological activity of the compounds derived from it, making it valuable in the development of active ingredients for crop protection. In pharmaceutical research, it is employed in the creation of molecules with potential therapeutic effects, especially in the design of drugs targeting specific enzymes or receptors. Its nitro group also allows for further functionalization, enabling the synthesis of diverse chemical entities for various applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white to light yellow Solid |
| PURITY | 96.5-100 |
| 1 H NMR Spectrum | Consistent with structure |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft17,238.57 |
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| 1.000 | 10-20 days | Ft53,762.80 |
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2-(2-Nitro-4-(trifluoromethyl)phenyl)acetonitrile
This chemical is primarily utilized in the synthesis of various agrochemicals and pharmaceuticals due to its unique structural properties. It serves as a key intermediate in the production of herbicides and pesticides, particularly those targeting broadleaf weeds and pests in agricultural settings. Additionally, its trifluoromethyl group enhances the biological activity of the compounds derived from it, making it valuable in the development of active ingredients for crop protection. In pharmaceutical research, it is employed in the creation of molecules with potential therapeutic effects, especially in the design of drugs targeting specific enzymes or receptors. Its nitro group also allows for further functionalization, enabling the synthesis of diverse chemical entities for various applications.
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