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CS-W001157 4
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4-Chloro-6,7-difluoro-2-methylquinazoline

  • CAS No. 887592-02-1

  • Cat. No. CS-0152747
  • Purity≥97%
  • MDL No.MFCD06657231

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

4-Chloro-6,7-difluoro-2-methylquinazoline|CS-0152747

Structure of 887592-02-1

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General Information

  • CAS No. 887592-02-1
  • Cat. No. CS-0152747
  • Purity ≥97%
  • MDL No. MFCD06657231
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₅ClF₂N₂
  • Molecular Weight 214.60
  • Synonym(s) None
  • SMILES CC1=NC2=CC(=C(C=C2C(=N1)Cl)F)F

Description

4-Chloro-6,7-difluoro-2-methylquinazoline features a highly electron-deficient quinazoline core with strategic halogen and methyl substitutions. This scaffold enables direct integration into medicinal chemistry campaigns, particularly for kinase inhibitor development. The difluoro substitution enhances metabolic stability while the chloro group provides a reactive handle for palladium-catalyzed coupling. Bench-stable and moisture-tolerant, it simplifies handling in diverse synthetic workflows.

Application

4-Chloro-6,7-difluoro-2-methylquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient access to kinase inhibitor scaffolds. Its electron-deficient quinazoline core facilitates nucleophilic substitution reactions, particularly at the C4-chloro position, and exhibits excellent bench stability. The 6,7-difluoro substitution enhances metabolic stability and modulates electronic properties, while the 2-methyl group provides steric control during downstream functionalization. This compound functions effectively in standard coupling protocols and is well-suited for parallel synthesis campaigns targeting biologically active heterocycles.

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-H320-H335
Precautionary Statements : P264-P270-P330

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Computational Chemistry Data

  • TPSA   25.78
  • LogP   2.86982
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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