m-Tolylboronic acid

97%

Reagent Code: #90243
label
Alias 3-Methylphenylboronic acid ;3-Methylphenylboronic acid
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CAS Number 17933-03-8

science Other reagents with same CAS 17933-03-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.96 g/mol
Formula C₇H₉BO₂
badge Registry Numbers
MDL Number MFCD00040198
thermostat Physical Properties
Melting Point 160-162 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

m-Tolylboronic 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. It serves as a key intermediate in the production of various biaryl compounds, which are crucial in drug development and material science. Additionally, it is employed in the preparation of liquid crystals and organic electronic materials due to its ability to introduce aryl groups into target molecules. Its versatility and stability make it a valuable reagent in modern synthetic chemistry.

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Test Parameter Specification
Purity 96.5-103.5%
Appearance White to off-white solid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,400.00
inventory 1g
10-20 days ฿380.00
inventory 5g
10-20 days ฿500.00
inventory 100g
10-20 days ฿5,500.00

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m-Tolylboronic acid
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m-Tolylboronic 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. It serves as a key intermediate in the production of various biaryl compounds, which are crucial in drug development and material science. Additionally, it is employed in the preparation of liquid crystals and organi

m-Tolylboronic 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. It serves as a key intermediate in the production of various biaryl compounds, which are crucial in drug development and material science. Additionally, it is employed in the preparation of liquid crystals and organic electronic materials due to its ability to introduce aryl groups into target molecules. Its versatility and stability make it a valuable reagent in modern synthetic chemistry.

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