| Identification | Back Directory | [Name]
QUINOLINE-2-CARBONITRILE | [CAS]
1436-43-7 | [Synonyms]
Quinaldonitrile
2-Cyanoquinoline
Quinolinecarbonitrile
quinolin-2-carbonitrile
2-QUINOLINECARBONITRILE
QUINOLINE-2-CARBONITRILE
Quinoline-2-Carbinitrile
2-Quinolinecarbonitrile ,97%
Quinoline-2-carbonitrile 97%
QUINOLINE-2-CARBONITRILE ISO 9001：2015 REACH | [EINECS(EC#)]
215-865-1 | [Molecular Formula]
C10H6N2 | [MDL Number]
MFCD00134341 | [MOL File]
1436-43-7.mol | [Molecular Weight]
154.17 |
| Chemical Properties | Back Directory | [Melting point ]
93-95 °C(lit.)
| [Boiling point ]
160°C 23mm | [density ]
1.21 | [refractive index ]
1.4820 (estimate) | [Fp ]
160°C/23mm | [storage temp. ]
Inert atmosphere,Room Temperature | [pka]
-0.56±0.40(Predicted) | [Water Solubility ]
Insoluble in water. | [BRN ]
115213 |
| Hazard Information | Back Directory | [Uses]
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. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 81, p. 4004, 1959 DOI: 10.1021/ja01524a046 | [General Description]
Mechanism of the photoinduced substitution reaction of 2-quinolinecarbonitrile in alcohols or ethers has been reported. Photoinitiated dimerization of 2-quinolinecarbonitrile in HCl-acidified 2-propanol/water has been investigated at 77K and 331K. Benzophenone-sensitization of 2-quinolinecarbonitrile has been reported to yield triazapentaphene. |
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