(4-Bromo-3-chlorophenyl)boronic acid
98%
Reagent
Code: #87104
CAS Number
1217501-28-4
blur_circular Chemical Specifications
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Molecular Information
Weight
235.27 g/mol
Formula
C₆H₅BBrClO₂
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Registry Numbers
MDL Number
MFCD12913945
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Physical Properties
Boiling Point
361.8±52.0 °C(Predicted)
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Storage & Handling
Density
1.79±0.1 g/cm3(Predicted)
Storage
room temperature, inert gas
description 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.
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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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