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CS-W001157 4
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6-Bromo-4-chloro-2-methylquinazoline

  • CAS No. 351426-04-5

  • Cat. No. CS-W018935
  • Molecule weight257.51
  • Purity≥96%
  • MDL No.MFCD06657210

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

6-Bromo-4-chloro-2-methylquinazoline|CS-W018935

Structure of 351426-04-5

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General Information

  • CAS No. 351426-04-5
  • Cat. No. CS-W018935
  • Purity ≥96%
  • MDL No. MFCD06657210
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₆BrClN₂
  • Molecular Weight 257.51
  • Synonym(s) 6-BROMO-4-CHLORO-2-METHYL-QUINAZOLINE
  • SMILES BrC2=CC=C1N=C(N=C(C1=C2)Cl)C

Description

6-Bromo-4-chloro-2-methylquinazoline features a sterically accessible quinazoline core with complementary halogenation and methyl substitution. This configuration enables direct functionalization in cross-coupling reactions, delivering diverse heterocyclic architectures under standard conditions. The electron-deficient ring system enhances reactivity in Pd-catalyzed transformations while maintaining bench-stable handling properties.

Application

6-Bromo-4-chloro-2-methylquinazoline serves as a versatile building block for the synthesis of kinase inhibitors and other bioactive heterocycles. Its complementary halogenation pattern enables palladium-catalyzed cross-coupling reactions with high efficiency, while the methyl group provides a site for further functionalization. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for both medicinal chemistry and process-scale applications.

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   25.78
  • LogP   3.35412
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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