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CS-W001157 4
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Quinazoline-8-carbaldehyde

  • CAS No. 1823899-37-1

  • Cat. No. CS-0187977
  • Purity≥98%
  • MDL No.None

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

Quinazoline-8-carbaldehyde|CS-0187977

Structure of 1823899-37-1

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General Information

  • CAS No. 1823899-37-1
  • Cat. No. CS-0187977
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₆N₂O
  • Molecular Weight 158.16
  • Synonym(s) 8-Quinazolinecarboxaldehyde
  • SMILES O=CC1=CC=CC=2C=NC=NC12

Description

Quinazoline-8-carbaldehyde serves as a key heterocyclic scaffold for medicinal chemistry applications, featuring a reactive aldehyde group at the 8-position that enables facile conjugation. This functionalization supports efficient derivatization in drug discovery campaigns targeting kinase inhibitors and other bioactive molecules. The compound exhibits stability under standard bench conditions and compatibility with diverse reaction environments.

Application

Quinazoline-8-carbaldehyde serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling direct functionalization at the C8 position via imine formation, reductive amination, or nucleophilic addition. Its aldehyde functionality exhibits excellent bench stability and compatibility with diverse reaction conditions, facilitating efficient access to quinazoline-based scaffolds used in kinase inhibitor development and API intermediate construction.

Safety Information

Download SDS
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   42.85
  • LogP   1.4423
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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