4-Bromo-2-nitro-5-(trifluoromethyl)aniline
97%
- Product Code: 79508
CAS:
683241-86-3
| Molecular Weight: | 285.02 g./mol | Molecular Formula: | C₇H₄BrF₃N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09263997 | |
| Melting Point: | Boiling Point: | 310.7±42.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
Used primarily in the synthesis of complex organic compounds, this chemical serves as a key intermediate in the production of agrochemicals and pharmaceuticals. Its structure, featuring a nitro group and a trifluoromethyl group, makes it valuable in creating compounds with specific biological activities. In agrochemicals, it is often employed to develop herbicides and pesticides that target specific plant or pest pathways. In pharmaceuticals, it is utilized in the synthesis of active ingredients for drugs, particularly those requiring unique electronic properties due to the presence of the trifluoromethyl group. Additionally, its bromo substituent allows for further functionalization, enabling the creation of diverse derivatives for research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿702.00 |
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| 0.250 | 10-20 days | ฿999.00 |
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| 1.000 | 10-20 days | ฿2,043.00 |
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| 5.000 | 10-20 days | ฿8,901.00 |
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4-Bromo-2-nitro-5-(trifluoromethyl)aniline
Used primarily in the synthesis of complex organic compounds, this chemical serves as a key intermediate in the production of agrochemicals and pharmaceuticals. Its structure, featuring a nitro group and a trifluoromethyl group, makes it valuable in creating compounds with specific biological activities. In agrochemicals, it is often employed to develop herbicides and pesticides that target specific plant or pest pathways. In pharmaceuticals, it is utilized in the synthesis of active ingredients for drugs, particularly those requiring unique electronic properties due to the presence of the trifluoromethyl group. Additionally, its bromo substituent allows for further functionalization, enabling the creation of diverse derivatives for research and industrial applications.
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