4-Methyl-2-Nitro-1-(Trifluoromethyl)Benzene
≥98%
- Product Code: 79903
CAS:
154057-13-3
| Molecular Weight: | 205.13 g./mol | Molecular Formula: | C₈H₆F₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16140172 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure, featuring a nitro group and a trifluoromethyl group, makes it valuable in the development of active pharmaceutical ingredients (APIs) that require specific electron-withdrawing properties. Additionally, it plays a role in the production of agrochemicals, where it contributes to the creation of herbicides and pesticides with enhanced efficacy. In material science, it is utilized in the synthesis of specialty chemicals and polymers, particularly those requiring stability and resistance to degradation. Its applications also extend to research and development, where it serves as a building block for exploring new chemical reactions and pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿5,868.00 |
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4-Methyl-2-Nitro-1-(Trifluoromethyl)Benzene
This chemical is primarily used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure, featuring a nitro group and a trifluoromethyl group, makes it valuable in the development of active pharmaceutical ingredients (APIs) that require specific electron-withdrawing properties. Additionally, it plays a role in the production of agrochemicals, where it contributes to the creation of herbicides and pesticides with enhanced efficacy. In material science, it is utilized in the synthesis of specialty chemicals and polymers, particularly those requiring stability and resistance to degradation. Its applications also extend to research and development, where it serves as a building block for exploring new chemical reactions and pathways.
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