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CS-W001157 4
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4-Chloro-7-fluoroquinazoline

  • CAS No. 16499-62-0

  • Cat. No. CS-D0286
  • Purity≥96%
  • MDL No.MFCD08236729

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

4-Chloro-7-fluoroquinazoline|CS-D0286

Structure of 16499-62-0

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General Information

  • CAS No. 16499-62-0
  • Cat. No. CS-D0286
  • Purity ≥96%
  • MDL No. MFCD08236729
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₄ClFN₂
  • Molecular Weight 182.58
  • Synonym(s) 4-CHLORO-7-FLUORO-QUINAZOLINE
  • SMILES FC1=CC2=NC=NC(Cl)=C2C=C1

Description

4-Chloro-7-fluoroquinazoline delivers a highly reactive scaffold for medicinal chemistry, combining electron-deficient aromaticity with orthogonal functional handles. This bench-stable heterocycle enables direct coupling and cyclization strategies in kinase inhibitor development, where halogen substitution enhances binding affinity and metabolic stability.

Application

4-Chloro-7-fluoroquinazoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 4- and 7-positions via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its orthogonal reactivity profile supports the construction of diverse quinazoline-based scaffolds with high regiocontrol. The molecule exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard synthetic workflows for API development and target-oriented synthesis.

Synthesis

  • Route1

    References

    • Huang, Kenneth He; Veal, James; Barta, Thomas; Smith, Emilie D.; Ma, Wei; Ommen, Andy Patent: US2008/70935 A1, 2008 ; Location in patent: Page/Page column 54 ;

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   2.4223
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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