Quinoline-2-carbonitrile, 97%
Quinoline-2-carbonitrile, 97%
Quinoline-2-carbonitrile, 97%
Thermo Scientific Chemicals

Quinoline-2-carbonitrile, 97%

CAS: 1436-43-7 | C10H6N2 | 154.17 g/mol
Quantity:
1 g
5 g
Catalog number L19427.06
Price (JPY)
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Quantity:
5 g
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Chemical Identifiers
CAS1436-43-7
IUPAC Namequinoline-2-carbonitrile
Molecular FormulaC10H6N2
InChI KeyWDXARTMCIRVMAE-UHFFFAOYSA-N
SMILESN#CC1=CC=C2C=CC=CC2=N1
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder
Melting Point (clear melt)90.0-99.0?C
Appearance (Color)White to cream to yellow
Assay (GC)≥96.0%
Quinoline-2-carbonitrile is used to produce quinoline-2-carboxylic acid amide. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

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.

Applications
Quinoline-2-carbonitrile is used to produce quinoline-2-carboxylic acid amide. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Solubility
Insoluble in water.

Notes
Store in a cool, dry conditions in well sealed container. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Norisuke Hata; Tsugio Saito. The Photochemistry of 2-Quinolinecarbonitriles. II. A Mechanism of the Photoinduced Substitution Reaction. Bulletin of the Chemical Society of Japan.1974, 47, (4), 942-945.
  2. Tullio Caronna; Sergio Morrocchi; Bruno M. Vittimberga. Photoinitiated radical-forming reactions of 2-quinolinecarbonitrile at 77 and 331 K. J. Org. Chem.1981, 46, (1), 34-38.