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Tetrahydroquinoline information


Tetrahydroquinoline
Names
Preferred IUPAC name
1,2,3,4-Tetrahydroquinoline
Other names
Hydroquinoline
Identifiers
CAS Number
  • 635-46-1
3D model (JSmol)
  • Interactive image
Beilstein Reference
116149
ChEBI
  • CHEBI:213323
ChEMBL
  • ChEMBL303611
ChemSpider
  • 62667
ECHA InfoCard 100.010.216 Edit this at Wikidata
EC Number
  • 211-237-6
Gmelin Reference
27202
PubChem CID
  • 69460
UNII
  • CCR50N1Z9G
CompTox Dashboard (EPA)
  • DTXSID8060903 Edit this at Wikidata
InChI
  • InChI=1S/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h1-2,4,6,10H,3,5,7H2
    Key: LBUJPTNKIBCYBY-UHFFFAOYSA-N
SMILES
  • C1CC2=CC=CC=C2NC1
Properties
Chemical formula
C9H11N
Molar mass 133.194 g·mol−1
Appearance Colorless oily liquid
Density 1.0599 g/cm3
Melting point 20 °C (68 °F; 293 K)
Boiling point 251 °C (484 °F; 524 K)
Hazards
GHS labelling:
Pictograms
GHS07: Exclamation markGHS08: Health hazard
Signal word
Danger
Hazard statements
H315, H319, H335, H350
Precautionary statements
P201, P202, P261, P264, P271, P280, P281, P302+P352, P304+P340, P305+P351+P338, P308+P313, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
Related compounds
Related compounds
Quinoline, Tetralin, Chromane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Tetrahydroquinoline is an organic compound that is the semi-hydrogenated derivative of quinoline. It is a colorless oil.

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(link). Chen, Fei (2015). "Synthesis of Optically Active 1,2,3,4-Tetrahydroquinolines via Asymmetric Hydrogenation Using Iridium-Diamine Catalyst". Org...

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P, Fischmeister R, et al. (December 2012). "Identification of a tetrahydroquinoline analog as a pharmacological inhibitor of the cAMP-binding protein...

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Povarov reaction

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scandium(III) triflate catalyzed conditions to yield cyclopropane-fused tetrahydroquinolines in good yields and diastereoselectivities. Treatment of these compounds...

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