4-Carboxy-2-Nitrophenylboronic Acid

95%

Reagent Code: #90720
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CAS Number 85107-54-6

science Other reagents with same CAS 85107-54-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.94 g/mol
Formula C₇H₆BNO₆
badge Registry Numbers
MDL Number MFCD00448780
thermostat Physical Properties
Melting Point 265-268°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It is also employed in the development of sensors and probes for detecting sugars and other biologically relevant molecules due to its boronic acid group, which can selectively bind to diols. Additionally, it finds application in the preparation of pharmaceutical intermediates and in materials science for modifying surfaces or creating functionalized polymers. Its nitro group enhances its reactivity, making it useful in various catalytic and analytical processes.

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

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inventory 1g
10-20 days ฿1,590.00

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4-Carboxy-2-Nitrophenylboronic Acid
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Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It is also employed in the development of sensors and probes for detecting sugars and other biologically relevant molecules due to its boronic acid group, which can selectively bind to diols. Additionally, it finds application in the preparation of pharmaceutical intermediates and in materials science for modifying surfaces or creating functionalized polymers. Its nitro group e

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It is also employed in the development of sensors and probes for detecting sugars and other biologically relevant molecules due to its boronic acid group, which can selectively bind to diols. Additionally, it finds application in the preparation of pharmaceutical intermediates and in materials science for modifying surfaces or creating functionalized polymers. Its nitro group enhances its reactivity, making it useful in various catalytic and analytical processes.

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