(3-Methoxy-2-methylphenyl)boronic acid
97%
Reagent
Code: #118158
CAS Number
1313617-76-3
blur_circular Chemical Specifications
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Molecular Information
Weight
165.98 g/mol
Formula
C₈H₁₁BO₃
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Registry Numbers
MDL Number
MFCD18398348
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Physical Properties
Boiling Point
325.8±52.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, protected from light, stored in an inert gas
description Product Description
(3-Methoxy-2-methylphenyl)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 synthesis 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 sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in biochemical and analytical applications. Its stability and reactivity also make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive compounds.
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(3-Methoxy-2-methylphenyl)boronic acid
(3-Methoxy-2-methylphenyl)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 synthesis 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 sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in biochemical and analytical applications. Its stability and reactivity also make it a preferred choice in medicinal chemistry for designing drug candidates and bioactive compounds.
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