4-Carboxy-3-chlorobenzeneboronic acid
97%
Reagent
Code: #90723
Alias
4-Carboxy-3-chlorophenylboronic acid
3-Chloro-4-carboxyphenylboronic acid
CAS Number
136496-72-5
blur_circular Chemical Specifications
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Molecular Information
Weight
200.38 g/mol
Formula
C₇H₆BClO₄
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Registry Numbers
MDL Number
MFCD06656268
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Physical Properties
Melting Point
236-238
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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 |
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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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