Indolizine

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Structural formula
Structural formula of indolizine
General
Surname Indolizine
other names

Pyrrolo [1,2-a] pyridine

Molecular formula C 8 H 7 N
Brief description

colorless solid

External identifiers / databases
CAS number 274-40-8
EC number 691-518-1
ECHA InfoCard 100.219.195
PubChem 9230
ChemSpider 8875
Wikidata Q910641
properties
Molar mass 117.15 g mol −1
Physical state

firmly

Melting point

75 ° C

boiling point

205 ° C

solubility
  • practically insoluble in water
  • soluble in ethanol
safety instructions
GHS hazard labeling
no classification available
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Indolizine is a chemical compound from the group of heteroaromatic bicyclic compounds having bridgehead - nitrogen atom.

Occurrence

Indolizine occurs naturally as the basic structure of many alkaloids ( e.g. rotundifoline , leurosine , eburnine , Catharanthus alkaloids ).

Extraction and presentation

Indolizine is formed when 2-methylpyridine is heated with α-bromoacetaldehyde and during the decarboxylation of indolizine-2-carboxylic acid , which is accessible from 2-methylpyridine and α-bromopyruvic acid.

properties

Indolizine is in the form of naphthalene- smelling, colorless flakes, which are easily soluble in organic solvents, and are soluble in warm dilute acids with gradual decomposition. It is steam volatile. The hydrochloric acid solution turns a spruce wood chip red, its solutions in benzene fluoresce strongly violet.

Individual evidence

  1. a b c Lexicon of Chemistry: Indolizin - Lexikon der Chemie , accessed on May 28, 2020
  2. a b c d David R. Lide: CRC Handbook of Chemistry and Physics A Ready-reference Book of Chemical and Physical Data . CRC Press, 1995, ISBN 978-0-8493-0595-5 , pp. 332 ( limited preview in Google Book search).
  3. This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
  4. Eberhard Breitmeier, Günther Jung: Organic chemistry . Basics, substance classes, reactions, concepts, molecular structure. 5th edition. Georg Thieme Verlag, Stuttgart 2005, ISBN 3-13-541505-8 , p. 698 ( limited preview in Google Book search).

Web links

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