5,6-Dimethoxyindole structure
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Common Name | 5,6-Dimethoxyindole | ||
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CAS Number | 14430-23-0 | Molecular Weight | 177.200 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 320.3±22.0 °C at 760 mmHg | |
Molecular Formula | C10H11NO2 | Melting Point | 154-157 °C(lit.) | |
MSDS | USA | Flash Point | 117.4±12.6 °C |
Name | 5,6-dimethoxyindole |
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Synonym | More Synonyms |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 320.3±22.0 °C at 760 mmHg |
Melting Point | 154-157 °C(lit.) |
Molecular Formula | C10H11NO2 |
Molecular Weight | 177.200 |
Flash Point | 117.4±12.6 °C |
Exact Mass | 177.078979 |
PSA | 34.25000 |
LogP | 1.82 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.609 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi: Irritant; |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
Precursor 9 | |
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DownStream 6 | |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
[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-glyoxala... |
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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-dimet... |
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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 p... |
1H-Indole, 5,6-dimethoxy- |
5,6-Dimethoxyindole |
MFCD00005675 |
5,6-Dimethoxy-1H-indole |
EINECS 238-402-5 |