(3-Bromo-2-methylphenyl)boronic acid

95%

Reagent Code: #36683
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CAS Number 1184298-27-8

science Other reagents with same CAS 1184298-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.85 g/mol
Formula C₇H₈BBrO₂
badge Registry Numbers
MDL Number MFCD18447597
inventory_2 Storage & Handling
Storage -20℃, inert gas

description Product Description

(3-Bromo-2-methylphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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 introduction of the (3-bromo-2-methylphenyl) group into target structures. Its boronic acid functionality allows for efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is used in the development of bioactive compounds and in research focused on creating novel chemical entities for drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,242.00
inventory 250mg
10-20 days ฿2,700.00
inventory 5g
10-20 days ฿32,040.00

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(3-Bromo-2-methylphenyl)boronic acid
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(3-Bromo-2-methylphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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 introduction of the (3-bromo-2-methylphenyl) group into target structures. Its boronic acid functionality allows for efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is used in the development of bioactive compounds and in research focused on creating novel chemical entities for drug discovery.
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