4-Carboxy-3-chlorobenzeneboronic acid

97%

Reagent Code: #90723
label
Alias 4-Carboxy-3-chlorophenylboronic acid 3-Chloro-4-carboxyphenylboronic acid
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CAS Number 136496-72-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.38 g/mol
Formula C₇H₆BClO₄
badge Registry Numbers
MDL Number MFCD06656268
thermostat Physical Properties
Melting Point 236-238
inventory_2 Storage & Handling
Density 0.88 g/cm
Storage 2~8°C

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. This compound is also employed in the development of sensors and materials for detecting specific analytes due to its boronic acid group, which can interact with diols and other functional groups. Additionally, it finds application in the research and production of bioactive compounds, including potential drug candidates targeting diseases such as cancer and diabetes. Its versatility makes it a useful tool in medicinal chemistry and material science.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97-100
Appearance White crystal powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿580.00
inventory 5g
10-20 days ฿2,690.00
4-Carboxy-3-chlorobenzeneboronic acid
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex organic molecules. This compound is also employed in the development of sensors and materials for detecting specific analytes due to its boronic acid group, which can interact with diols and other functional groups. Additionally, it finds application in the research and production of bioactive compounds, including potential drug candidates targeting diseases such as cancer and diabetes. Its versatility makes it a useful tool in medicinal chemistry and material science.
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