4-Benzoylphenylboronic acid

98%

Reagent Code: #90744
label
Alias 4-Benzoylphenylboronic acid
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CAS Number 268218-94-6

science Other reagents with same CAS 268218-94-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.04 g/mol
Formula C₁₃H₁₁BO₃
badge Registry Numbers
MDL Number MFCD05664212
thermostat Physical Properties
Melting Point 204-212 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8 ℃

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes for detecting sugars and other biomolecules due to its ability to form reversible complexes with diols. In material science, it is utilized in the creation of organic electronic devices and polymers, contributing to the advancement of flexible electronics and optoelectronic materials. Its versatility and reactivity make it a crucial component in various research and industrial applications.

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Test Parameter Specification
Purity 97.5-100
Appearance Powder and/or chunks
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿740.00
inventory 1g
10-20 days ฿1,760.00
inventory 5g
10-20 days ฿5,640.00

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4-Benzoylphenylboronic acid
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes for detecting sugars and other biomolecules due to its ability to form reversible complexes with dio

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and probes for detecting sugars and other biomolecules due to its ability to form reversible complexes with diols. In material science, it is utilized in the creation of organic electronic devices and polymers, contributing to the advancement of flexible electronics and optoelectronic materials. Its versatility and reactivity make it a crucial component in various research and industrial applications.

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