Isoquinolina-1-carbonitrilo, 99 %, Thermo Scientific Chemicals

CAS: 1198-30-7 | C10H6N2 | 154.172 g/mol

Número de catálogo	Cantidad
L19425.03 también denominado L19425-03	1 g

Número de catálogo L19425.03

también denominado L19425-03

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Identificadores químicos

CAS1198-30-7

IUPAC Nameisoquinoline-1-carbonitrile

Molecular FormulaC10H6N2

InChI KeyHJHXYSBRTVFEDD-UHFFFAOYSA-N

SMILESN#CC1=C2C=CC=CC2=CC=N1

Especificaciones Specification Sheet

Appearance (Color)White to cream or pale yellow

Assay (GC)≥98.5%

FormCrystals or powder or crystalline powder or flakes

Identification (FTIR)Conforms

Isoquinoline-1-carbonitrile is used as starting reagent in the syntheses of imidazo[5,1-a]isoquinolines. It is also used as intermediate in organic syntheses.

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
La isoquinolin-1-carbonitrilo se utiliza como reactivo inicial en las síntesis de imidazo[5,1-a]isoquinolinas. También se utiliza como intermedio en síntesis orgánicas.

Solubilidad
Insoluble en agua.

Notas
Almacenar en un lugar fresco. Mantener el recipiente bien cerrado en un lugar seco y bien ventilado. Incompatible con agentes oxidantes.

RUO – Research Use Only

General References:

Sharmistha Dutta Choudhury.; Samita Basu. Interaction of 4-nitroquinoline-1-oxide with indole derivatives and some related biomolecules: a study with magnetic field. Journal of Physical Chemistry. 2006, 110 (17), 8850-8855.
Mickaël Pauvert.; Sylvain C. Colleta.; Marie-Jo Bertranda.; André Y. Guingant.; Michel Evain. Synthesis of chiral N-protected 1,2-dihydro-quinoline-2-carbonitrile and 1,2-dihydro-isoquinoline-1-carbonitrile via an asymmetric Reissert reaction. Tetrahedron Letters. 2005, 46 (17), 2983-2987.