(5-Methoxy-2-methylphenyl)boronic acid

97%

Reagent Code: #90920
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CAS Number 617689-07-3

science Other reagents with same CAS 617689-07-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.98 g/mol
Formula C₈H₁₁BO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(5-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, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the construction of complex aromatic compounds. Additionally, it is employed in the development of sensors and ligands due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿1,962.00
100mg
10-20 days ฿4,734.00
(5-Methoxy-2-methylphenyl)boronic acid
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(5-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, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the construction of complex aromatic compounds. Additionally, it is employed in the development of sensors and ligands due to its ability to interact with diols

(5-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, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the construction of complex aromatic compounds. Additionally, it is employed in the development of sensors and ligands due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications.

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