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CS-W001157 4
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6-Bromo-4-methylquinazoline

  • CAS No. 69674-27-7

  • Cat. No. CS-0233385
  • Purity≥98%
  • MDL No.None

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

6-Bromo-4-methylquinazoline|CS-0233385

Structure of 69674-27-7

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General Information

  • CAS No. 69674-27-7
  • Cat. No. CS-0233385
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₇BrN₂
  • Molecular Weight 223.07
  • Synonym(s) 6-bromanyl-4-methyl-quinazoline
  • SMILES CC1=C2C=C(C=CC2=NC=N1)Br

Description

6-Bromo-4-methylquinazoline is a heterocyclic scaffold featuring a bromine atom at the 6-position and a methyl group at the 4-position, enabling selective functionalization in medicinal chemistry. This electron-deficient core integrates readily into kinase inhibitor designs and serves as a key intermediate for constructing bioactive quinazoline derivatives under standard coupling conditions.

Application

6-Bromo-4-methylquinazoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biaryl and heteroaryl scaffolds. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl group enhances regiochemical control and metabolic stability. Its bench-stable crystalline form facilitates handling and purification, making it ideal for iterative synthesis campaigns targeting kinase inhibitors and other pharmaceutical candidates.

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-P330-P362-P405-P501

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Computational Chemistry Data

  • TPSA   25.78
  • LogP   2.70072
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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