Indoline
From Wikipedia, the free encyclopedia
| Indoline | |
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2,3-dihydro-1H-indole |
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Other names
2,3-Dihydroindole |
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| Identifiers | |
| CAS number | 496-15-1 |
| PubChem | 10328 |
| ChemSpider | 9905 |
| ChEBI | CHEBI:43295 |
| ChEMBL | CHEMBL388803 |
| RTECS number | NL6906300 |
| Beilstein Reference | 111915 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C8H9N |
| Appearance | Clear green liquid |
| Density | 1.063 g/mL |
| Melting point |
-21 °C |
| Boiling point |
220–221 °C |
| Hazards | |
| MSDS | Fisher Scientific |
| Related compounds | |
| Related aromatics | carbazole, indole, isoindoline, oxindole |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Indoline is an aromatic heterocyclic organic compound. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing ring. The compound is based on the indole structure, but the 2-3 bond is saturated. By oxidation/dehydrogenation it can be converted to indoles.
| This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it. |