Indolizine

Chemical compound From Wikipedia, the free encyclopedia

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 certain plant alkaloids such as swainsonine.[3]

Quick facts Names, Identifiers ...
Indolizine
Names
Preferred IUPAC name
Indolizine[1]
Other names
Pyrrocoline; Indolizin; Pyrrolo[1,2-a]pyridine
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.219.195 Edit this at Wikidata
UNII
  • InChI=1S/C8H7N/c1-2-6-9-7-3-5-8(9)4-1/h1-7H checkY
    Key: HOBCFUWDNJPFHB-UHFFFAOYSA-N checkY
  • InChI=1/C8H7N/c1-2-6-9-7-3-5-8(9)4-1/h1-7H
    Key: HOBCFUWDNJPFHB-UHFFFAOYAH
  • c1ccc2ccccn12
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 [2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Examples of some simple fully synthetic substituted indolizines include 2ZEDMA, 1ZP2MA, and 1Z2MAP1O.[4][5]

References

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