3-Acetylphenylboronic acid

96%

Reagent Code: #90119
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Alias 3-Acetylphenylboronic acid
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CAS Number 204841-19-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.97 g/mol
Formula CH₃COC₆H₄BOH₂
badge Registry Numbers
MDL Number MFCD01074678
thermostat Physical Properties
Melting Point 204-208 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

3-Acetylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. 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 due to its ability to interact with diols and other functional groups, facilitating the detection of biological molecules. Its acetyl group further enhances its versatility by allowing derivatization for specific applications in drug discovery and material science.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 206-210
Purity (HPLC) 96-100
Appearance White to pale yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days £613.70
inventory 25g
10-20 days £154.00
inventory 1g
10-20 days £8.96
inventory 5g
10-20 days £31.03
3-Acetylphenylboronic acid
3-Acetylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. 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 due to its ability to interact with diols and other functional groups, facilitating the detection of biological molecules. Its acetyl group further enhances its versatility by allowing derivatization for specific applications in drug discovery and material science.
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