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Details

Stereochemistry ACHIRAL
Molecular Formula C9H6ClN
Molecular Weight 163.604
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-CHLOROQUINOLINE

SMILES

ClC1=CC=C2C=CC=CC2=N1

InChI

InChIKey=OFUFXTHGZWIDDB-UHFFFAOYSA-N
InChI=1S/C9H6ClN/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H

HIDE SMILES / InChI

Molecular Formula C9H6ClN
Molecular Weight 163.604
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
N-[(2-Chloro-3-quinol-yl)meth-yl]-4-fluoro-aniline.
2010-09-11
4-Chloro-2,5-dimethyl-quinoline.
2010-07-14
1-{6-Chloro-2-[(2-chloro-8-methyl-3-quinol-yl)meth-oxy]-4-phenyl-quinolin-3-yl}ethanone.
2010-07-07
1-{6-Chloro-2-[(2-chloro-6-methyl-quinolin-3-yl)meth-oxy]-4-phenyl-quinolin-3-yl}ethanone.
2010-06-18
1-{6-Chloro-2-[(2-chloro-3-quinol-yl)meth-oxy]-4-phenyl-3-quinol-yl}ethan-1-one.
2010-06-09
Synthesis and in vitro biological evaluation of carbon-11-labeled quinoline derivatives as new candidate PET radioligands for cannabinoid CB2 receptor imaging.
2010-03-15
Chemoenzymatic synthesis of chiral 2,2'-bipyridine ligands and their N-oxide derivatives: applications in the asymmetric aminolysis of epoxides and asymmetric allylation of aldehydes.
2010-03-07
Chemicals possessing a neurotrophin-like activity on dopaminergic neurons in primary culture.
2009-07-10
The identification of nonpeptide neurotensin receptor partial agonists from the potent antagonist SR48692 using a calcium mobilization assay.
2009-03-01
Azaarene cis-dihydrodiol-derived 2,2'-bipyridine ligands for asymmetric allylic oxidation and cyclopropanation.
2008-11-21
N-(2-Chloro-quinolin-3-ylmethyl-ene)aniline.
2007-12-12
Sensitive and rapid liquid chromatography/tandem mass spectrometric assay for the quantification of piperaquine in human plasma.
2007-11-01
Sensitive and rapid liquid chromatography/tandem mass spectrometric assay for the quantification of chloroquine in dog plasma.
2007-06-01
Chloroquinolines block antibiotic efflux pumps in antibiotic-resistant Enterobacter aerogenes isolates.
2006-06
Use of highly active palladium-phosphinous acid catalysts in Stille, Heck, amination, and thiation reactions of chloroquinolines.
2003-09-05
Novel synthesis of 2-chloroquinolines from 2-vinylanilines in nitrile solvent.
2002-11-01
Synthesis of 1,4-disubstituted 2-methylpiperazine derivatives, new 5-HT(1A) receptor ligands.
2002-03-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:43:33 GMT 2025
Edited
by admin
on Mon Mar 31 18:43:33 GMT 2025
Record UNII
UX7RIN8GEW
Record Status Validated (UNII)
Record Version
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Name Type Language
2-CHLOROQUINOLINE
Systematic Name English
NSC-6163
Preferred Name English
CHLOROQUINOLINE, 2-
Systematic Name English
Code System Code Type Description
FDA UNII
UX7RIN8GEW
Created by admin on Mon Mar 31 18:43:33 GMT 2025 , Edited by admin on Mon Mar 31 18:43:33 GMT 2025
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CAS
612-62-4
Created by admin on Mon Mar 31 18:43:33 GMT 2025 , Edited by admin on Mon Mar 31 18:43:33 GMT 2025
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ECHA (EC/EINECS)
210-317-8
Created by admin on Mon Mar 31 18:43:33 GMT 2025 , Edited by admin on Mon Mar 31 18:43:33 GMT 2025
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NSC
6163
Created by admin on Mon Mar 31 18:43:33 GMT 2025 , Edited by admin on Mon Mar 31 18:43:33 GMT 2025
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PUBCHEM
11928
Created by admin on Mon Mar 31 18:43:33 GMT 2025 , Edited by admin on Mon Mar 31 18:43:33 GMT 2025
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EPA CompTox
DTXSID8060612
Created by admin on Mon Mar 31 18:43:33 GMT 2025 , Edited by admin on Mon Mar 31 18:43:33 GMT 2025
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WIKIPEDIA
2-Chloroquinoline
Created by admin on Mon Mar 31 18:43:33 GMT 2025 , Edited by admin on Mon Mar 31 18:43:33 GMT 2025
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