Indoline

from Wikipedia, the free encyclopedia
Structural formula
Structural formula of indoline
General
Surname Indoline
other names
  • 2,3-dihydro-1 H -indole
  • 1H -indoline
  • 1-azaindan
  • Benzopyrrolidine
Molecular formula C 8 H 9 N
Brief description

colorless liquid at room temperature

External identifiers / databases
CAS number 496-15-1
EC number 207-816-8
ECHA InfoCard 100.007.107
PubChem 10328
Wikidata Q2613101
properties
Molar mass 119.16376 g mol −1
Physical state

liquid

density

1.069 g cm −3

boiling point

230 ° C

solubility
  • soluble in organic solvents
  • slightly soluble in water
Refractive index

1.5922

safety instructions
GHS labeling of hazardous substances
07 - Warning
H and P phrases H: 302-315-319-335
P: 261-305 + 351 + 338-302 + 352-321-405-501
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C

Indoline is a chemical substance and occurs as a structural fragment in many natural substances .

presentation

Indoline can be prepared by reduction of the indole with zinc dust and 85% hydrochloric acid are shown. In contrast to earlier syntheses, there is hardly any polymerization as a side reaction.

use

Indoline is used in the manufacture of pharmaceuticals and dyes.

Individual evidence

  1. a b c d e f Entry on indoline. In: Römpp Online . Georg Thieme Verlag, accessed on June 14, 2014.
  2. T. Tóth, Á. Gerecs: Indole and Indole Derivatives, IX in Acta Chimica Hungarica: a Journal of the Hungarian Academy of Sciences , 67, No. 2, 1971, pp. 229-239
  3. a b data sheet indoline at AlfaAesar, accessed on May 4, 2013 ( PDF )(JavaScript required) .
  4. Lloyd J. Dolby, Gordon W. Gribble : A convenient preparation of indoline . In: Journal of Heterocyclic Chemistry . tape 3 , no. 2 , June 1966, p. 124–125 , doi : 10.1002 / jhet.5570030202 (English, PDF ).