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CS-W001157 4
Total: USD 88.00

2-Acetyl-6-bromopyridine

  • CAS No. 49669-13-8

  • Cat. No. CS-W002593
  • Purity≥97%
  • MDL No.MFCD00272200

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

2-Acetyl-6-bromopyridine|CS-W002593

Structure of 49669-13-8

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General Information

  • CAS No. 49669-13-8
  • Cat. No. CS-W002593
  • Purity ≥97%
  • MDL No. MFCD00272200
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₆BrNO
  • Molecular Weight 200.03
  • Synonym(s) None
  • SMILES CC(C1=NC(Br)=CC=C1)=O

Description

2-Acetyl-6-bromopyridine features a bromine atom at the 6-position and an acetyl group at the 2-position, creating a sterically accessible, electron-deficient pyridine scaffold. This dual-functionalized heterocycle integrates readily into cross-coupling reactions and serves as a key intermediate in synthesizing bioactive nitrogen-containing compounds under standard conditions.

Application

2-Acetyl-6-bromopyridine serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The acetyl group provides a handle for selective functionalization, including enolization and nucleophilic addition. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for constructing complex heterocyclic scaffolds and advanced intermediates in medicinal chemistry 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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501

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Computational Chemistry Data

  • TPSA   29.96
  • LogP   2.0467
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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