Indolizine

From Wikipedia, the free encyclopedia
Indolizine
Indolizin - Indolizine.svg
Indolizine ball-and-stick.png
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
  • 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).
checkY  (what is checkY☒N ?)
Infobox references

Indolizine (Chemical formula C8H7N) is a heterocyclic aromatic organic compound that is an isomer of indole. The saturated analog indolizidine forms the structural core of a variety of alkaloids such as swainsonine.

Weight[]

The known molar mass of C8H7N is 117.151 g/mol.[3]

Properties[]

The following is a list of both physical and chemical properties:

Physical properties[]

References[]

  1. ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 213. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. ^ Elattar, K.M.; Youssef, I.; Fadda, A.A. (4 May 2016). "Reactivity of indolizines in organic synthesis". Synthetic Communications Reviews. 46 (9): 719–744. doi:10.1080/00397911.2016.1166252.
  3. ^ "Indolizine".

External links[]


Stub icon

This article about a heterocyclic compound is a stub. You can help Wikipedia by .

  • v
  • t
Retrieved from ""