5,6-二甲氧基吲哚
5,6-二甲氧基吲哚结构式
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常用名 | 5,6-二甲氧基吲哚 | 英文名 | 5,6-Dimethoxyindole |
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| CAS号 | 14430-23-0 | 分子量 | 177.200 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 320.3±22.0 °C at 760 mmHg | |
| 分子式 | C10H11NO2 | 熔点 | 154-157 °C(lit.) | |
| MSDS | 美版 | 闪点 | 117.4±12.6 °C |
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[Monoamine oxidase inhibitors. I. Synthesis of N-cyclopropyltryptamines].
Farmaco. Sci. 35(9) , 785-90, (1980) The synthesis of two new N-cyclopropyltryptamines is described. By treating 5,6-dimethoxyindole with oxalyl chloride and N-benzylcyclopropylamine, N-benzyl-N-cyclopropyl-5,6-dimethoxyindole-3-glyoxalamide is obtained. The reduction of this compound by LiAlH4,... |
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Cross-polarization dynamics and spin diffusion in some aromatic compounds.
Solid State Nucl. Magn. Reson. 3(3) , 121-35, (1994) The inversion-recovery cross-polarization (IRCP) magic-angle spinning experiment has been applied to study the 13C-1H cross-polarization dynamics of protonated aromatic carbons in ferrocene, 5,6-dimethoxyindole (DMI) and some indole derivatives. Using the 13C... |
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Structural characterization of two isomeric dimethoxyindoles of biological interest, using high- and low-energy collisional spectroscopy.
Rapid Commun. Mass Spectrom. 3(12) , 413-6, (1989) It is not possible to distinguish isomers of biologically important dimethoxyindoles using electron-ionization mass spectra, but they may be distinguished by collisionally activated dissociation. In particular, energy-resolved mass spectrometry yields the bes... |