Indolizine
| Names | |
|---|---|
| Preferred IUPAC name
Indolizine | |
| Other names
Pyrrocoline; Indolizin; Pyrrolo[1,2-a]pyridine | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.219.195 |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C8H7N | |
| Molar mass | 117.151 g·mol−1 |
| Appearance | White solid |
| Melting point | 75 °C (167 °F; 348 K) |
| Boiling point | 205 °C (401 °F; 478 K) |
| Basicity (pKb) | 10.1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Indolizine is an heterocyclic compound with the formula C8H7N). It is an uncommon isomer of indole with the nitrogen located at a ring fusion position. The saturated analog is indolizidine, which is the core of a variety of alkaloids such as swainsonine.
Examples of some simple fully synthetic substituted indolizines include 2ZEDMA, 1ZP2MA, and 1Z2MAP1O.