3-Chloro-4-methylphenylboronic acid

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Reagent Code: #90211
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Alias 3-Chloro-4-methylphenylboronic acid
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CAS Number 175883-63-3

science Other reagents with same CAS 175883-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.4 g/mol
Formula C₇H₈BClO₂
badge Registry Numbers
MDL Number MFCD04039010
thermostat Physical Properties
Melting Point 210-216°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

3-Chloro-4-methylphenylboronic 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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.

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Test Parameter Specification
Melting point 223-230
Purity (HPLC) 97-100
Appearance White crystalline powder
Infrared Spectrum Conforms

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿570.00
inventory 5g
10-20 days ฿1,760.00
inventory 25g
10-20 days ฿6,740.00

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3-Chloro-4-methylphenylboronic acid
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3-Chloro-4-methylphenylboronic 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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the crea

3-Chloro-4-methylphenylboronic 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. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.

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