(4-Bromo-3-chlorophenyl)boronic acid
98%
- Product Code: 87104
CAS:
1217501-28-4
Molecular Weight: | 235.27 g./mol | Molecular Formula: | C₆H₅BBrClO₂ |
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EC Number: | MDL Number: | MFCD12913945 | |
Melting Point: | Boiling Point: | 361.8±52.0 °C(Predicted) | |
Density: | 1.79±0.1 g/cm3(Predicted) | Storage Condition: | room temperature, inert gas |
Product Description:
(4-Bromo-3-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, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, enabling the creation of diverse chemical structures. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides, making it a versatile reagent in medicinal chemistry for drug discovery and development. Additionally, it is employed in the preparation of functionalized aromatic compounds used in organic electronics and materials science.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,422.00 |
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1.000 | 10-20 days | ฿3,843.00 |
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(4-Bromo-3-chlorophenyl)boronic acid
(4-Bromo-3-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, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, enabling the creation of diverse chemical structures. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides, making it a versatile reagent in medicinal chemistry for drug discovery and development. Additionally, it is employed in the preparation of functionalized aromatic compounds used in organic electronics and materials science.
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