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CS-W001157 4
Total: USD 88.00

2,4-Dichloro-7-nitroquinazoline

  • CAS No. 129112-65-8

  • Cat. No. CS-0141014
  • Purity≥95%
  • MDL No.MFCD18157742

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

2,4-Dichloro-7-nitroquinazoline|CS-0141014

Structure of 129112-65-8

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General Information

  • CAS No. 129112-65-8
  • Cat. No. CS-0141014
  • Purity ≥95%
  • MDL No. MFCD18157742
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₃Cl₂N₃O₂
  • Molecular Weight 244.03
  • Synonym(s) None
  • SMILES O=[N+](C1=CC2=NC(Cl)=NC(Cl)=C2C=C1)[O-]

Description

2,4-Dichloro-7-nitroquinazoline features a highly electron-deficient quinazoline core with dual chloro substituents at positions 2 and 4, enhancing reactivity for nucleophilic substitution. The para-nitro group at position 7 further increases electrophilicity, enabling efficient coupling in heterocyclic synthesis. This compound serves as a key scaffold for developing kinase inhibitors and advanced pharmaceutical intermediates under standard bench conditions.

Application

2,4-Dichloro-7-nitroquinazoline serves as a versatile building block in medicinal chemistry, enabling regioselective functionalization at the C2 and C4 positions via palladium-catalyzed cross-coupling reactions. Its electron-deficient quinazoline core enhances reactivity in nucleophilic substitution processes, while the nitro group provides a handle for reduction and downstream derivatization. The compound exhibits good bench stability and facilitates the construction of complex heterocyclic scaffolds relevant to kinase inhibitor development.

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+P364-P405-P501

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Computational Chemistry Data

  • TPSA   68.92
  • LogP   2.8448
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   1

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