5-Chloro-2-methylbenzeneboronic acid

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Reagent Code: #90893
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Alias 5-Chloro-2-methylphenylboronic acid
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CAS Number 148839-33-2

science Other reagents with same CAS 148839-33-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.4 g/mol
Formula C₇H₈BClO₂
badge Registry Numbers
MDL Number MFCD03411939
thermostat Physical Properties
Melting Point 162-166
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound facilitates the synthesis of biaryl compounds, which are essential in pharmaceuticals, agrochemicals, and organic materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) and in research for drug discovery, particularly in constructing molecules with potential therapeutic properties. Its stability and reactivity also make it suitable for use in polymer chemistry and material science for designing advanced functional materials.

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Test Parameter Specification
Purity (HPLC) 98-100
Purity (Neutralization Titration) 97-112
APPEARANCE White to off-white powder or solid or chunks
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿900.00
inventory 25g
10-20 days ฿4,230.00

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5-Chloro-2-methylbenzeneboronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound facilitates the synthesis of biaryl compounds, which are essential in pharmaceuticals, agrochemicals, and organic materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) and in research for drug discovery, particularly in constructing molecules with

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound facilitates the synthesis of biaryl compounds, which are essential in pharmaceuticals, agrochemicals, and organic materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) and in research for drug discovery, particularly in constructing molecules with potential therapeutic properties. Its stability and reactivity also make it suitable for use in polymer chemistry and material science for designing advanced functional materials.

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