3-(Benzylcarbamoyl)phenyl)boronic acid

98%

Reagent Code: #90283
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CAS Number 625470-96-4

science Other reagents with same CAS 625470-96-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.08 g/mol
Formula C₁₄H₁₄BNO₃
badge Registry Numbers
MDL Number MFCD04115688
thermostat Physical Properties
Melting Point 224-230°C
inventory_2 Storage & Handling
Density 1.24g/mL
Storage  2-8°C

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules. Its boronic acid group enables it to act as a coupling partner in these reactions, facilitating the formation of carbon-carbon bonds. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿30,240.00

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3-(Benzylcarbamoyl)phenyl)boronic acid
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Used in organic synthesis as a key intermediate for the preparation of various biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules. Its boronic acid group enables it to act as a coupling partner in these reactions, facilitating the formation of carbon-carbon bonds. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with d

Used in organic synthesis as a key intermediate for the preparation of various biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to create complex molecules. Its boronic acid group enables it to act as a coupling partner in these reactions, facilitating the formation of carbon-carbon bonds. Additionally, it is utilized in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it useful in biochemical and analytical applications.

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