(6-Aminopyridin-3-yl)boronic acid
95%
Reagent
Code: #90954
CAS Number
851524-96-4
blur_circular Chemical Specifications
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Molecular Information
Weight
137.93 g/mol
Formula
C₅H₇BN₂O₂
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Registry Numbers
MDL Number
MFCD09907980
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Physical Properties
Boiling Point
388.3°C
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Storage & Handling
Storage
2-8°C
description Product Description
(6-Aminopyridin-3-yl)boronic acid is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the construction of complex molecules with high precision. Additionally, it is employed in the development of bioactive compounds and drug candidates, where its aminopyridine moiety can enhance binding affinity to biological targets. Its role in catalysis and material science further highlights its versatility in industrial and research applications.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | White to off-white to pale yellow to yellow-brown solid |
| Purity | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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