2-CHLOROQUINOLINE

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 Search

SMILES

ClC1=NC2=C(C=CC=C2)C=C1

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

Title	Date	PubMed
Synthesis of 1,4-disubstituted 2-methylpiperazine derivatives, new 5-HT(1A) receptor ligands.	2001 Sep-Oct	11876443
Novel synthesis of 2-chloroquinolines from 2-vinylanilines in nitrile solvent.	2002 Nov 1	12398521
Use of highly active palladium-phosphinous acid catalysts in Stille, Heck, amination, and thiation reactions of chloroquinolines.	2003 Sep 5	12946152
Chloroquinolines block antibiotic efflux pumps in antibiotic-resistant Enterobacter aerogenes isolates.	2006 Jun	16707249
N-(2-Chloro-quinolin-3-ylmethyl-ene)aniline.	2007 Dec 12	21200823
Sensitive and rapid liquid chromatography/tandem mass spectrometric assay for the quantification of chloroquine in dog plasma.	2007 Jun 1	17317340
Sensitive and rapid liquid chromatography/tandem mass spectrometric assay for the quantification of piperaquine in human plasma.	2007 Nov 1	17923446
Azaarene cis-dihydrodiol-derived 2,2'-bipyridine ligands for asymmetric allylic oxidation and cyclopropanation.	2008 Nov 21	18997943
Chemicals possessing a neurotrophin-like activity on dopaminergic neurons in primary culture.	2009 Jul 10	19593444
The identification of nonpeptide neurotensin receptor partial agonists from the potent antagonist SR48692 using a calcium mobilization assay.	2009 Mar 1	19195889
4-Chloro-2,5-dimethyl-quinoline.	2010 Jul 14	21588331
1-{6-Chloro-2-[(2-chloro-8-methyl-3-quinol-yl)meth-oxy]-4-phenyl-quinolin-3-yl}ethanone.	2010 Jul 7	21588259
1-{6-Chloro-2-[(2-chloro-6-methyl-quinolin-3-yl)meth-oxy]-4-phenyl-quinolin-3-yl}ethanone.	2010 Jun 18	21587915
1-{6-Chloro-2-[(2-chloro-3-quinol-yl)meth-oxy]-4-phenyl-3-quinol-yl}ethan-1-one.	2010 Jun 9	21587841
Synthesis and in vitro biological evaluation of carbon-11-labeled quinoline derivatives as new candidate PET radioligands for cannabinoid CB2 receptor imaging.	2010 Mar 15	20189815
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 Mar 7	20165798
N-[(2-Chloro-3-quinol-yl)meth-yl]-4-fluoro-aniline.	2010 Sep 11	21587537

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:16:56 GMT 2023` Edited by `admin` on `Fri Dec 15 17:16:56 GMT 2023`
Record UNII	UX7RIN8GEW
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

2-CHLOROQUINOLINE

Systematic Name

English

NSC-6163

Code

English

CHLOROQUINOLINE, 2-

Systematic Name

English

Code System Code Type Description

FDA UNII

UX7RIN8GEW