3-tert-Butylphenylboronic acid

98%

Reagent Code: #90123
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CAS Number 560132-24-3

science Other reagents with same CAS 560132-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.04 g/mol
Formula C₁₀H₁₅BO₂
badge Registry Numbers
MDL Number MFCD11110647
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block in the development of sensors and catalysts due to its boronic acid group, which can selectively bind to diols and other functional groups. Additionally, it is employed in the preparation of advanced polymers and coatings, enhancing their stability and performance.

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Test Parameter Specification
Appearance White to Yellow 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 ฿600.00
inventory 5g
10-20 days ฿2,880.00
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3-tert-Butylphenylboronic acid
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block in the development of sensors and catalysts due to its boronic acid group, which can selectively bind to diols and other functional groups. Additionally, it is employed in the preparation of advanced polymers and coatings, enhancing their stability and performanc

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block in the development of sensors and catalysts due to its boronic acid group, which can selectively bind to diols and other functional groups. Additionally, it is employed in the preparation of advanced polymers and coatings, enhancing their stability and performance.

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