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Indolizine

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Indolizine
Names
Preferred IUPAC name Indolizine
Other names Pyrrocoline; Indolizin; Pyrrolopyridine
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.219.195 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C8H7N/c1-2-6-9-7-3-5-8(9)4-1/h1-7HKey: HOBCFUWDNJPFHB-UHFFFAOYSA-N
  • InChI=1/C8H7N/c1-2-6-9-7-3-5-8(9)4-1/h1-7HKey: HOBCFUWDNJPFHB-UHFFFAOYAH
SMILES
  • c1ccc2ccccn12
Properties
Chemical formula C8H7N
Molar mass 117.151 g·mol
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 , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

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 analogs are indolizidine, which are found in a variety of alkaloids such as swainsonine.

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. S2CID 100777050.
  3. Julio Alvarez-Builla; Juan Jose Vaquero; José Barluenga, eds. (2011). Modern Heterocyclic Chemistry. Wiley-VCH.

External links


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