4-Bromo-2-methylphenylboronic acid

95%

Reagent Code: #90659
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CAS Number 221006-71-9

science Other reagents with same CAS 221006-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.9 g/mol
Formula C₇H₈BBrO₂
badge Registry Numbers
MDL Number MFCD16660270
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

4-Bromo-2-methylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl halides or triflates in the presence of a palladium catalyst. Additionally, it serves as a building block in the development of bioactive compounds and functional polymers. Its stability and reactivity make it a valuable reagent in medicinal chemistry for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿549.00
inventory 1g
10-20 days ฿1,746.00

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4-Bromo-2-methylphenylboronic acid
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4-Bromo-2-methylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl halides or triflates in the presence of a palladium catalyst. Additionally, it serves as a building block in t

4-Bromo-2-methylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl halides or triflates in the presence of a palladium catalyst. Additionally, it serves as a building block in the development of bioactive compounds and functional polymers. Its stability and reactivity make it a valuable reagent in medicinal chemistry for drug discovery and development.

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