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CS-W001157 4
Total: USD 88.00

(6-Acetamidopyridin-3-yl)boronic acid

  • CAS No. 947533-21-3

  • Cat. No. CS-0092048
  • Purity≥95%
  • MDL No.MFCD09951917

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

(6-Acetamidopyridin-3-yl)boronic acid|CS-0092048

Structure of 947533-21-3

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General Information

  • CAS No. 947533-21-3
  • Cat. No. CS-0092048
  • Purity ≥95%
  • MDL No. MFCD09951917
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₉BN₂O₃
  • Molecular Weight 179.97
  • Synonym(s) 2-Acetamidopyridine-5-boronic acid
  • SMILES OB(C1=CN=C(NC(C)=O)C=C1)O

Description

This boronate moiety integrates a pyridine scaffold with an acetamido group, enabling selective functionalization in late-stage diversification. The electron-deficient ring enhances reactivity in Suzuki-Miyaura couplings, while the bench-stable boronic acid functionality simplifies handling and storage under standard conditions.

Application

(6-Acetamidopyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The pyridine core provides favorable electronic and steric properties for transition metal catalysis, while the acetamido group enhances solubility and offers a handle for further derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in the synthesis of functionalized heterocycles and pharmaceutical intermediates.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302
Precautionary Statements : P264-P270-P330-P501

Quality Control

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Computational Chemistry Data

  • TPSA   82.45
  • LogP   -1.2802
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   2

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