(6-Aminopyridin-3-yl)boronic acid

95%

  • Product Code: 90954
  CAS:    851524-96-4
Molecular Weight: 137.93 g./mol Molecular Formula: C₅H₇BN₂O₂
EC Number: MDL Number: MFCD09907980
Melting Point: Boiling Point: 388.3°C
Density: Storage Condition: 2-8°C
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.
Product Specification:
Test 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
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿700.00
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1.000 10-20 days ฿1,300.00
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(6-Aminopyridin-3-yl)boronic acid
(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.
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