Indoline

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Indoline
Indoline
Indoline
Other names
Identifiers
CAS number496-15-1 YesY
PubChem10328
ChemSpider9905 YesY
ChEBICHEBI:43295 YesY
ChEMBLChEMBL388803 YesY
RTECS numberNL6906300
111915
Jmol-3D imagesImage
Properties
C8H9N
Molar mass119.16 g/mol
AppearanceClear colourless liquid
Density1.063 g/mL
Melting point−21 °C (−6 °F; 252 K)
Boiling point220 to 221 °C (428 to 430 °F; 493 to 494 K)
Hazards
MSDSFisher Scientific
Flash point92.8 °C (199.0 °F; 365.9 K)
Related compounds
Related aromatics
carbazole, indole, isoindoline, oxindole
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY verify (what isYesY/N?)
Infobox references
 
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Indoline
Indoline
Indoline
Other names
Identifiers
CAS number496-15-1 YesY
PubChem10328
ChemSpider9905 YesY
ChEBICHEBI:43295 YesY
ChEMBLChEMBL388803 YesY
RTECS numberNL6906300
111915
Jmol-3D imagesImage
Properties
C8H9N
Molar mass119.16 g/mol
AppearanceClear colourless liquid
Density1.063 g/mL
Melting point−21 °C (−6 °F; 252 K)
Boiling point220 to 221 °C (428 to 430 °F; 493 to 494 K)
Hazards
MSDSFisher Scientific
Flash point92.8 °C (199.0 °F; 365.9 K)
Related compounds
Related aromatics
carbazole, indole, isoindoline, oxindole
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY verify (what isYesY/N?)
Infobox references

Indoline is an aromatic heterocyclic organic compound. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing ring. The compound is based on the indole structure, but the 2-3 bond is saturated. By oxidation/dehydrogenation it can be converted to indoles.[1][2]

References[edit]

  1. ^ Katritzky, A. R.; Pozharskii, A. F. (2000). Handbook of Heterocyclic Chemistry (2nd ed.). Academic Press. ISBN 0080429882. 
  2. ^ Clayden, J.; Greeves, N.; Warren, S.; Wothers, P. (2001). Organic Chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.