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CS-W001157 4
Total: USD 88.00

4-Chloro-6,7-difluoroquinazoline

  • CAS No. 625080-60-6

  • Cat. No. CS-W022153
  • Purity≥98%
  • MDL No.MFCD06657230

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

4-Chloro-6,7-difluoroquinazoline|CS-W022153

Structure of 625080-60-6

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General Information

  • CAS No. 625080-60-6
  • Cat. No. CS-W022153
  • Purity ≥98%
  • MDL No. MFCD06657230
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₃ClF₂N₂
  • Molecular Weight 200.57
  • Synonym(s) 4-chloro-6,7-difluoro-quinazoline
  • SMILES ClC1=NC=NC2=CC(=C(C=C12)F)F

Description

4-Chloro-6,7-difluoroquinazoline features a highly electron-deficient quinazoline core with orthogonal halogen substituents enabling selective cross-coupling. This bench-stable scaffold integrates readily into bioactive molecules, serving as a key building block for kinase inhibitors and pharmaceutical intermediates.

Application

4-Chloro-6,7-difluoroquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of kinase inhibitors and other bioactive heterocycles. The chloro group at the 4-position facilitates palladium-catalyzed cross-coupling reactions, while the 6,7-difluoro substitution enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for iterative synthesis campaigns and API development.

Synthesis

  • Route1

    References

    • AMBIT BIOSCIENCES CORPORATON Patent: WO2009/117080 A1, 2009 ; Location in patent: Page/Page column 165 ; WO 2009/117080 A1

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   25.78
  • LogP   2.5614
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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