N-Methyl-2-nitro-4-(trifluoromethyl)aniline
98%
- Product Code: 52580
CAS:
20200-22-0
| Molecular Weight: | 220.1486 g./mol | Molecular Formula: | C₈H₇F₃N₂O₂ |
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| EC Number: | MDL Number: | MFCD00798375 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
N-Methyl-2-nitro-4-(trifluoromethyl)aniline is primarily utilized in the field of organic synthesis as a key intermediate in the production of various agrochemicals and pharmaceuticals. Its unique structure, featuring both nitro and trifluoromethyl groups, makes it a valuable building block for the development of compounds with specific biological activities. In agrochemical applications, it is often employed in the synthesis of herbicides and pesticides, where the trifluoromethyl group enhances the compound's effectiveness and stability. In the pharmaceutical industry, it serves as a precursor in the creation of molecules with potential therapeutic properties, particularly in the design of drugs targeting specific enzymes or receptors. Additionally, its nitro group can be reduced to form amines, which are versatile intermediates in further chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | €18.52 |
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N-Methyl-2-nitro-4-(trifluoromethyl)aniline
N-Methyl-2-nitro-4-(trifluoromethyl)aniline is primarily utilized in the field of organic synthesis as a key intermediate in the production of various agrochemicals and pharmaceuticals. Its unique structure, featuring both nitro and trifluoromethyl groups, makes it a valuable building block for the development of compounds with specific biological activities. In agrochemical applications, it is often employed in the synthesis of herbicides and pesticides, where the trifluoromethyl group enhances the compound's effectiveness and stability. In the pharmaceutical industry, it serves as a precursor in the creation of molecules with potential therapeutic properties, particularly in the design of drugs targeting specific enzymes or receptors. Additionally, its nitro group can be reduced to form amines, which are versatile intermediates in further chemical transformations.
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