(3-Bromo-2-methylphenyl)boronic acid
95%
Reagent
Code: #36683
CAS Number
1184298-27-8
blur_circular Chemical Specifications
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Molecular Information
Weight
214.85 g/mol
Formula
C₇H₈BBrO₂
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Registry Numbers
MDL Number
MFCD18447597
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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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