(3-Bromo-4-chlorophenyl)boronic acid
95%
- Product Code: 123629
CAS:
1384956-55-1
| Molecular Weight: | 235.27 g./mol | Molecular Formula: | C₆H₅BBrClO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19981540 | |
| Melting Point: | Boiling Point: | 361.4±52.0 °C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
(3-Bromo-4-chlorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of bioactive compounds and as a building block in medicinal chemistry for drug discovery. Its unique structure, with bromo and chloro substituents, also makes it useful in designing molecules with specific electronic and steric properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,079.00 |
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| 0.250 | 10-20 days | ฿3,996.00 |
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(3-Bromo-4-chlorophenyl)boronic acid
(3-Bromo-4-chlorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is employed in the development of bioactive compounds and as a building block in medicinal chemistry for drug discovery. Its unique structure, with bromo and chloro substituents, also makes it useful in designing molecules with specific electronic and steric properties.
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