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CS-W001157 4
Total: USD 88.00

3-Bromo-5-fluoropyridin-2(1H)-one

  • CAS No. 884494-94-4

  • Cat. No. CS-0102949
  • Purity≥97%
  • MDL No.MFCD08277253

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

3-Bromo-5-fluoropyridin-2(1H)-one|CS-0102949

Structure of 884494-94-4

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General Information

  • CAS No. 884494-94-4
  • Cat. No. CS-0102949
  • Purity ≥97%
  • MDL No. MFCD08277253
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₃BrFNO
  • Molecular Weight 191.99
  • Synonym(s) 3-Bromo-5-fluoropyridin-2-OL
  • SMILES O=C1C(Br)=CC(F)=CN1

Description

3-Bromo-5-fluoropyridin-2(1H)-one features a fused heterocyclic core bearing strategically positioned halogen substituents, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The electron-deficient pyridinone scaffold enhances reactivity toward amines and thiols, while the bromine and fluorine atoms provide orthogonal handles for sequential derivatization. This bench-stable compound integrates readily into complex molecular architectures used in medicinal chemistry and materials science.

Application

3-Bromo-5-fluoropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal reactivity profile. The bromo group facilitates C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the fluorine and lactam functionalities provide enhanced metabolic stability and hydrogen-bonding capacity. Its bench-stable crystalline nature simplifies handling and purification, making it ideal for modular synthesis of bioactive heterocycles and API 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-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   32.86
  • LogP   1.2765
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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