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CS-W001157 4
Total: USD 88.00

2-Chloro-4-phenylquinazoline

  • CAS No. 29874-83-7

  • Cat. No. CS-W019034
  • Purity≥98%
  • MDL No.MFCD01152724

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

2-Chloro-4-phenylquinazoline|CS-W019034

Structure of 29874-83-7

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General Information

  • CAS No. 29874-83-7
  • Cat. No. CS-W019034
  • Purity ≥98%
  • MDL No. MFCD01152724
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₉ClN₂
  • Molecular Weight 240.69
  • Synonym(s) oro-4-phenyL
  • SMILES ClC1=NC(C2=CC=CC=C2)=C3C=CC=CC3=N1

Description

2-Chloro-4-phenylquinazoline delivers a robust heterocyclic scaffold for medicinal chemistry, featuring a chlorine atom at the C2 position and a phenyl group at C4. This substitution pattern enhances metabolic stability and facilitates targeted interactions in kinase inhibition studies. The compound exhibits excellent bench stability and solubility in common organic solvents, enabling seamless integration into synthetic workflows.

Application

2-Chloro-4-phenylquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinazoline-based scaffolds through palladium-catalyzed cross-coupling reactions. Its chlorine substituent at the 2-position provides high reactivity in Suzuki-Miyaura and Buchwald-Hartwig couplings, facilitating rapid diversification of the core structure. The phenyl group at C4 enhances planarity and π-stacking potential, contributing to favorable binding interactions in kinase inhibitor design. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses of targeted pharmaceutical candidates.

Safety Information

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GHS Pictogram :
GHS No : GHS06
Signal Word : Danger
UN#: 2811
Class : 6.1
Packing Group : Ⅲ
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   3.9502
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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