(3-Bromo-4-chlorophenyl)boronic acid

95%

Reagent Code: #123629
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CAS Number 1384956-55-1

science Other reagents with same CAS 1384956-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.27 g/mol
Formula C₆H₅BBrClO₂
badge Registry Numbers
MDL Number MFCD19981540
thermostat Physical Properties
Boiling Point 361.4±52.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,996.00
100mg
10-20 days ฿2,079.00
(3-Bromo-4-chlorophenyl)boronic acid
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(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

(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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