4-Aminophenylboronic acid pinacol ester

98%

Reagent Code: #90619
label
Alias 4-Aminophenylboronic acid pinacol ester 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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CAS Number 214360-73-3

science Other reagents with same CAS 214360-73-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.09 g/mol
Formula C₁₂H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD02093721
thermostat Physical Properties
Melting Point 165-169 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. These compounds are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block for designing sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars. Applied in the development of glucose-sensitive devices for diabetes management. Additionally, it plays a role in the preparation of advanced polymers and functionalized materials.

format_list_bulleted Product Specification

Test Parameter Specification
Carbon 63.5-68.1
Melting point 166-170
Nitrogen 6.1-6.6
Purity 98-100
Appearance White to brown crystals or powder chunks
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿360.00
inventory 5g
10-20 days ฿1,060.00
inventory 25g
10-20 days ฿4,350.00

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4-Aminophenylboronic acid pinacol ester
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. These compounds are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block for designing sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars. Applied in the development of glucose-sensitive devices for diabetes management. Additionally, it plays a role in the preparation of advanced

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. These compounds are essential in pharmaceuticals, agrochemicals, and materials science. It also serves as a building block for designing sensors and probes due to its boronic acid group, which can selectively bind to diols and sugars. Applied in the development of glucose-sensitive devices for diabetes management. Additionally, it plays a role in the preparation of advanced polymers and functionalized materials.

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