Quinolina-2-carboxaldehído, 97 %, Thermo Scientific Chemicals
Quinolina-2-carboxaldehído, 97 %, Thermo Scientific Chemicals
Quinolina-2-carboxaldehído, 97 %, Thermo Scientific Chemicals
Quinolina-2-carboxaldehído, 97 %, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Quinolina-2-carboxaldehído, 97 %, Thermo Scientific Chemicals

CAS: 5470-96-2 | C10H7NO | 157.17 g/mol
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Cantidad:
5 g
25 g
Número de catálogo L20202.14
también denominado L20202-14
Precio (USD)
-
Cantidad:
25 g
Pedido a granel o personalizado
Identificadores químicos
CAS5470-96-2
EspecificacionesSpecification SheetHoja de especificaciones
FormCrystals or powder or crystalline powder
Free acid (titration)≤1.5%
Assay (GC)≥96.0%
Melting Point64.0-70.0?C
Appearance (Color)Yellow to orange to brown
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 acetophenone; imine-type ligands; sugar-quinoline fluorescent sensor for the detection of Hg2+ in natural water.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El 2-quinolinacarboxaldehído se utilizó en la preparación de 3-(2-quinolil)-1-fenil-2-propenona mediante reacciones rápidas y en tándem de aldol-Michael con los enolatos de litio, sodio y potasio de acetofenona; ligandos tipo imina; sensor fluorescente de azúcar-quinolina para la detección de Hg2+ en agua natural.

Solubilidad
Insoluble en agua.

Notas
Estable en las condiciones de almacenamiento recomendadas. Incompatible con agentes oxidantes.
RUO – Research Use Only

General References:

  1. Wachter-Jurcsak N, et al. Addressing the unusual reactivity of 2-pyridinecarboxaldehyde and 2-quinolinecarboxaldehyde in base-catalyzed aldol reactions with acetophenone. Tetrahedron Lett.1998,39(23), 3903-6
  2. Attilio Ardizzoia G, et al. Copper (I)-imine complexes: Synthesis and catalytic activity in olefin cyclopropanation. Inorganica Chim. Acta.2009,362(10), 3507-12