2-Aminopyrimidine-5-boronic acid pinacol ester

96%

Reagent Code: #89878
label
Alias 2-aminopyrimidine-5-boronic acid pinadate
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CAS Number 402960-38-7

science Other reagents with same CAS 402960-38-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.06 g/mol
Formula C₁₀H₁₆BN₃O₂
badge Registry Numbers
MDL Number MFCD06795685
thermostat Physical Properties
Melting Point 209-211°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex molecules. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the synthesis of heterocyclic compounds, which are essential in drug discovery for targeting various diseases. Additionally, its stability and reactivity make it a preferred choice for constructing biologically active molecules and functionalized materials in research and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 96-100
Appearance White to pale yellow solid
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿880.00
250mg
10-20 days ฿490.00
5g
10-20 days ฿2,640.00
25g
10-20 days ฿10,880.00
2-Aminopyrimidine-5-boronic acid pinacol ester
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex molecules. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the synthesis of heterocyclic compounds, which are essential in drug discovery for targeting various diseases. Additionally, its stability and reactivity make it a preferred choice for constructing biologically active molecules and functionalized materials in research and industrial applications.
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