4-Bromo-3-(trifluoromethyl)aniline
98%
- Product Code: 72399
Alias:
4-Bromo-3-(trifluoromethyl)aniline
5-Amino-2-bromobenzotrifluoride
4-Amino-1-bromo-2-(trifluoromethyl)benzene
3-Trifluoromethyl-4-bromoaniline
CAS:
393-36-2
| Molecular Weight: | 240.02 g./mol | Molecular Formula: | C₇H₅BrF₃N |
|---|---|---|---|
| EC Number: | 206-885-1 | MDL Number: | MFCD00007827 |
| Melting Point: | 47-49 °C(lit.) | Boiling Point: | 81-84 °C0.5 mm Hg(lit.) |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of compounds with potential biological activity, particularly in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. Additionally, it is utilized in the creation of herbicides and pesticides due to its trifluoromethyl group, which enhances the stability and efficacy of these products. Its bromine substituent allows for further functionalization, making it a versatile building block in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 48-53 |
| PURITY GC | 98-100 |
| PURITYNONAQUEOUS TIERATION | 98.5-100 |
| APPEARANCE | WHITE TO ORANGE TO BROWN POWDER,CRYSTALS OR CHUNKS |
| INFRARED SPECTRUM | 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 |
|---|---|---|---|
| 1.000 | 10-20 days | $17.58 |
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| 5.000 | 10-20 days | $20.59 |
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| 25.000 | 10-20 days | $88.40 |
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4-Bromo-3-(trifluoromethyl)aniline
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of compounds with potential biological activity, particularly in the development of drugs targeting central nervous system disorders and anti-inflammatory agents. Additionally, it is utilized in the creation of herbicides and pesticides due to its trifluoromethyl group, which enhances the stability and efficacy of these products. Its bromine substituent allows for further functionalization, making it a versatile building block in organic synthesis.
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