4-Bromo-2-(trifluoromethyl)benzoic acid
98%
- Product Code: 143437
CAS:
320-31-0
| Molecular Weight: | 269.02 g./mol | Molecular Formula: | C₈H₄BrF₃O₂ |
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| EC Number: | MDL Number: | MFCD07787468 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for selective functionalization in drug design, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in agrochemicals for the production of herbicides and fungicides due to the electron-withdrawing nature of the trifluoromethyl group, which improves bioavailability and environmental persistence. Suitable for research in medicinal chemistry for structure-activity relationship (SAR) studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿148.50 |
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| 1.000 G | 10-20 days | ฿154.00 |
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| 5.000 G | 10-20 days | ฿450.00 |
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| 25.000 G | 10-20 days | ฿2,010.00 |
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| 500.000 G | 10-20 days | ฿36,880.00 |
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| 100.000 G | 10-20 days | ฿7,530.00 |
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4-Bromo-2-(trifluoromethyl)benzoic acid
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for selective functionalization in drug design, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build complex aromatic systems. Also utilized in agrochemicals for the production of herbicides and fungicides due to the electron-withdrawing nature of the trifluoromethyl group, which improves bioavailability and environmental persistence. Suitable for research in medicinal chemistry for structure-activity relationship (SAR) studies.
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