4-Isobutylphenylboronic Acid

≥98%

Reagent Code: #90568
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CAS Number 153624-38-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.04 g/mol
Formula C₁₀H₁₅BO₂
thermostat Physical Properties
Melting Point 117-120°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

4-Isobutylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient and selective coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with diols and other functional groups, making it useful in analytical and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days $163.57
4-Isobutylphenylboronic Acid
4-Isobutylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient and selective coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with diols and other functional groups, making it useful in analytical and industrial applications.
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