2-苯基吲哚-3-甲醛
2-苯基吲哚-3-甲醛结构式
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常用名 | 2-苯基吲哚-3-甲醛 | 英文名 | 2-phenylindole-3-carboxaldehyde |
|---|---|---|---|---|
| CAS号 | 25365-71-3 | 分子量 | 221.25400 | |
| 密度 | 1.237 g/cm3 | 沸点 | 462.9ºC at 760 mmHg | |
| 分子式 | C15H11NO | 熔点 | 249-253 °C(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 237.5ºC | |
| 符号 |
GHS07 |
信号词 | Warning |
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Synthesis of 2-arylindole derivatives and evaluation as nitric oxide synthase and NFκB inhibitors.
Org. Biomol. Chem. 10(44) , 8835-47, (2012) Development of small molecule drug-like inhibitors blocking both nitric oxide synthase and NFκB could offer a synergistic therapeutic approach in the prevention and treatment of inflammation and cancer. During the course of evaluating the biological potential... |
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Iridium-catalyzed regio- and enantioselective N-allylation of indoles.
Angew. Chem. Int. Ed. Engl. 48(42) , 7841-4, (2009)
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Novel indium-mediated ternary reactions between indole-3-carboxaldehydes-allyl bromide-enamines: facile synthesis of bisindolyl-and indolyl-heterocyclic alkanes. Kumar S, et al.
Tetrahedron Lett. 44(10) , 2101-2104, (2003)
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Acylation of indoles by Duff reaction and Vilsmeier-Haack formylation and conformation of N-formylindoles. Chatterjee A and Biswas KM.
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