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CS-W001157 4
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6-Bromo-8-chloro-4(3H)-quinazolinone

  • CAS No. 100949-34-6

  • Cat. No. CS-0654237
  • Molecule weight259.49
  • Purity≥98%
  • MDL No.None

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

6-Bromo-8-chloro-4(3H)-quinazolinone|CS-0654237

Structure of 100949-34-6

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General Information

  • CAS No. 100949-34-6
  • Cat. No. CS-0654237
  • Purity ≥98%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₄BrClN₂O
  • Molecular Weight 259.49
  • Synonym(s) None
  • SMILES O=C1NC=NC2=C1C=C(Br)C=C2Cl

Description

6-Bromo-8-chloro-4(3H)-quinazolinone features a fused bicyclic core with strategically positioned halogen substituents, enabling direct functionalization in transition-metal-catalyzed cross-coupling reactions. The electron-deficient quinazolinone scaffold supports efficient incorporation into bioactive molecule frameworks, particularly in kinase inhibitor development and medicinal chemistry lead optimization.

Application

6-Bromo-8-chloro-4(3H)-quinazolinone serves as a versatile building block for the synthesis of substituted quinazolinones, enabling efficient transition-metal-catalyzed cross-coupling reactions. Its dual halogen functionality offers orthogonal reactivity for sequential derivatization, while its bench-stable nature and compatibility with common reaction conditions facilitate straightforward purification and integration into medicinal chemistry campaigns.

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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362+P364

Quality Control

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Computational Chemistry Data

  • TPSA   45.75
  • LogP   2.339
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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