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CS-W001157 4
Total: USD 88.00

(5-Aminopyridin-3-yl)boronic acid

  • CAS No. 1169748-84-8

  • Cat. No. CS-0067147
  • Purity≥97%
  • MDL No.MFCD07374883

*For research and further manufacturing use only, not for direct human use.

(5-Aminopyridin-3-yl)boronic acid|CS-0067147

Structure of 1169748-84-8

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General Information

  • CAS No. 1169748-84-8
  • Cat. No. CS-0067147
  • Purity ≥97%
  • MDL No. MFCD07374883
  • Storage -20°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₇BN₂O₂
  • Molecular Weight 137.93
  • Synonym(s) 5-aminopyridin-3-ylboronic
  • SMILES OB(C1=CC(N)=CN=C1)O

Description

This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions, offering high functional group tolerance and stability under standard conditions. The 5-aminopyridin-3-yl scaffold provides enhanced solubility and facilitates downstream derivatization through amine-directed transformations.

Application

(5-Aminopyridin-3-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its amine-functionalized pyridine core provides enhanced solubility and facilitates downstream derivatization, while the boronic acid group exhibits excellent stability and compatibility with standard Suzuki-Miyaura conditions. Ideal for medicinal chemistry applications requiring nitrogen-rich heterocycles, it functions reliably in multi-step synthesis workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   79.37
  • LogP   -1.6564
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   1

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