(2-Aminopyridin-4-yl)boronic acid

97%

Reagent Code: #89046
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CAS Number 903513-62-2

science Other reagents with same CAS 903513-62-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.93 g/mol
Formula C₅H₇BN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, including potential drug candidates. Additionally, it finds applications in material science for designing advanced polymers and functional materials. Its role in catalysis and as a ligand in coordination chemistry also highlights its versatility in various chemical processes.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 96.5-100
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿630.00
100mg
10-20 days ฿1,251.00
250mg
10-20 days ฿2,115.00
1g
10-20 days ฿8,433.00
(2-Aminopyridin-4-yl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, including potential drug candidates. Additionally, it finds applications in material science for designing advanced

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for constructing complex molecules, especially in pharmaceutical research and development. The boronic acid group enables the formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, including potential drug candidates. Additionally, it finds applications in material science for designing advanced polymers and functional materials. Its role in catalysis and as a ligand in coordination chemistry also highlights its versatility in various chemical processes.

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