3-Amino-4-methylbenzeneboronic acid

98%

Reagent Code: #90182
label
Alias 3-Amino-4-methylphenylboronic acid
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CAS Number 22237-12-3

science Other reagents with same CAS 22237-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.98 g/mol
Formula C₇H₁₀BNO₂
badge Registry Numbers
EC Number 000-000-0
MDL Number MFCD01074640
thermostat Physical Properties
Melting Point 250°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as a building block for the creation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form biaryl compounds, which are essential in pharmaceuticals and material science. Additionally, its amino and boronic acid functional groups make it a versatile intermediate in the development of sensors and diagnostic agents, especially for detecting sugars and other biologically relevant molecules. Its applications also extend to the field of medicinal chemistry, where it is used in the synthesis of potential drug candidates targeting various diseases.

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Test Parameter Specification
Purity 98-100
Appearance White to yellow to brown to grey powder or chunks
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,160.00
inventory 5g
10-20 days ฿10,080.00

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3-Amino-4-methylbenzeneboronic acid
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This compound is primarily utilized in organic synthesis as a building block for the creation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form biaryl compounds, which are essential in pharmaceuticals and material science. Additionally, its amino and boronic acid functional groups make it a versatile intermediate in the development of sensors and diagnostic agents, especially for detecting sugars and other bi

This compound is primarily utilized in organic synthesis as a building block for the creation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form biaryl compounds, which are essential in pharmaceuticals and material science. Additionally, its amino and boronic acid functional groups make it a versatile intermediate in the development of sensors and diagnostic agents, especially for detecting sugars and other biologically relevant molecules. Its applications also extend to the field of medicinal chemistry, where it is used in the synthesis of potential drug candidates targeting various diseases.

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