2-Pyridinylacetonitrile
2-Pyridinylacetonitrile structure
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Common Name | 2-Pyridinylacetonitrile | ||
|---|---|---|---|---|
| CAS Number | 2739-97-1 | Molecular Weight | 118.136 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 232.1±15.0 °C at 760 mmHg | |
| Molecular Formula | C7H6N2 | Melting Point | 23-25°C | |
| MSDS | Chinese USA | Flash Point | 93.9±0.0 °C | |
| Symbol |
GHS06 |
Signal Word | Danger | |
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Self-assembled hybrid metal oxide base catalysts prepared by simply mixing with organic modifiers.
Nat. Commun. 6 , 8580, (2015) Multidentate materials formed by simply mixing heterogeneous and homogeneous components are promising for construction of versatile active sites on the surface of heterogeneous compounds, however, to the best of our knowledge, there are no reports on such mat... |
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Silver-Mediated Synthesis of Indolizines via Oxidative C-H functionalization and 5- endo-dig cyclization.
Tetrahedron Lett. 55(50) , 6922-6924, (2014) An efficient strategy for the synthesis of indolizines from readily available starting materials via oxidative C-H functionalization and 5-endo-dig cyclization in one step has been demonstrated. This protocol represents wide substrate scope, high functional g... |
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Acylation and other reactions of 2-and 4-pyridylacetonitrile. Gutsche CD and Voges HD.
J. Org. Chem. 32(9) , 2685-89, (1969)
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Studies with azinylacetonitriles: 2-pyridylacetonitrile as a precursor to functionally substituted pyridines.
Molecules 14(11) , 4406-13, (2009) 2-Pyridylacetonitrile (1) couples with aromatic diazonium salts to yield arylhydrazones 2a-c, that were shown to exist in the syn-form 2 rather than the anti-form 4. Compounds 2a,c reacted with hydroxylamine in refluxing DMF to yield the interesting 1,2,3-tri... |
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Synthesis of 1-cyano-2-hydroxy-4-quinolizinones and corresponding 5-cyano-4-hydroxy-2-pyridones. Part 187: Synthesis of heterocycles. Part 9: Quinolizines and Indolizines.
Pharmazie 32(5) , 278-9, (1977) Active malonic esters condense with 2-pyridylacetonitrile giving 1-cyano-3-substituted 2-hydroxyquinolizin-4-ones. Catalytic hydrogenation of the resulting products led to the corresponding 1-cyano-3-substituted-2-hydroxy-6.7.8.9-tetrahydroquinolizin-4-ones. ... |