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CS-W001157 4
Total: USD 88.00

Quinoline-2-carboxaldehyde

  • CAS No. 5470-96-2

  • Cat. No. CS-W008168
  • Purity≥98%
  • MDL No.MFCD00075032

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

Quinoline-2-carboxaldehyde|CS-W008168

Structure of 5470-96-2

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General Information

  • CAS No. 5470-96-2
  • Cat. No. CS-W008168
  • Purity ≥98%
  • MDL No. MFCD00075032
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₇NO
  • Molecular Weight 157.17
  • Synonym(s) 2-Quinolinecarboxaldehyde
  • SMILES O=CC1=NC2=CC=CC=C2C=C1

Description

2-Quinolinecarboxaldehyde was used in the preparation of:3-(2-quinolyl)-1-phenyl-2-propenone via rapid, tandem aldol-Michael reactions with the lithium, sodium and potassium enolates of acetophenoneimine-type ligandssugar-quinoline fluorescent sensor for the detection of Hg2+ in natural water

Application

Quinoline-2-carboxaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized pharmaceutical intermediates. Its aldehyde functionality exhibits reliable reactivity in imine formation, reductive amination, and transition-metal-catalyzed coupling reactions. The quinoline core provides inherent stability and π-conjugation, enhancing solubility and facilitating purification. This compound functions effectively in multi-step syntheses requiring orthogonality and bench-stable reagents.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501

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Computational Chemistry Data

  • TPSA   29.96
  • LogP   2.0473
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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