3-Chlorophenylboronic acid

97%

Reagent Code: #90217
label
Alias 3-Chlorophenylboronic acid; m-chlorophenylboronic acid
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CAS Number 63503-60-6

science Other reagents with same CAS 63503-60-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.37 g/mol
Formula C₆H₆BClO₂
badge Registry Numbers
MDL Number MFCD00161354
thermostat Physical Properties
Melting Point 185-189 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) and fine chemicals. Also employed in material science for developing organic electronic materials and polymers. Its boronic acid group enables it to form stable complexes with diols, making it useful in sensor development for detecting sugars and other biomolecules.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97-100
Melting Point 185-189
Appearance White to tan to red powder or chunks
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿360.00
inventory 25g
10-20 days ฿1,310.00
inventory 100g
10-20 days ฿5,020.00

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3-Chlorophenylboronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) and fine chemicals. Also employed in material science for developing organic electronic materials and polymers. Its boronic acid group enables it to form stable complexes with diols, making it useful in sensor development for detecting sugars and oth

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) and fine chemicals. Also employed in material science for developing organic electronic materials and polymers. Its boronic acid group enables it to form stable complexes with diols, making it useful in sensor development for detecting sugars and other biomolecules.

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