(3-Chloro-2-fluoro-5-(trifluoromethyl)phenyl)boronic acid
97%
- Product Code: 78965
CAS:
2096342-38-8
| Molecular Weight: | 242.36 g./mol | Molecular Formula: | C₇H₄BClF₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD25459282 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its unique structure, featuring a trifluoromethyl group and halogen substituents, makes it valuable for introducing specific functional groups into target compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) and advanced materials, where precise molecular modifications are required. Additionally, its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures, which are common in many drugs and organic materials.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,100.00 |
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| 1.000 | 10-20 days | ฿2,620.00 |
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| 5.000 | 10-20 days | ฿9,880.00 |
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(3-Chloro-2-fluoro-5-(trifluoromethyl)phenyl)boronic acid
This chemical is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its unique structure, featuring a trifluoromethyl group and halogen substituents, makes it valuable for introducing specific functional groups into target compounds. It is often employed in the development of active pharmaceutical ingredients (APIs) and advanced materials, where precise molecular modifications are required. Additionally, its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures, which are common in many drugs and organic materials.
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