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Details

Stereochemistry ACHIRAL
Molecular Formula C10H9NO
Molecular Weight 159.1846
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-METHYL-8-HYDROXYQUINOLINE

SMILES

CC1=NC2=C(C=CC=C2O)C=C1

InChI

InChIKey=NBYLBWHHTUWMER-UHFFFAOYSA-N
InChI=1S/C10H9NO/c1-7-5-6-8-3-2-4-9(12)10(8)11-7/h2-6,12H,1H3

HIDE SMILES / InChI

Molecular Formula C10H9NO
Molecular Weight 159.1846
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
THE IN VITRO EFFECT OF 8-HYDROXYQUINOLINE DERIVATIVES ON STRAINS OF MYCOBACTERIUM TUBERCULOSIS.
1964 Feb
Styrylquinoline derivatives: a new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells.
1998 Jul 16
Extraction equilibrium of palladium(II) with 2-methyl-8-quinolinol into supercritical carbon dioxide fluid.
2002 May 16
Solvent effect on distribution ratio of Pd(II) in supercritical carbon dioxide extraction and solvent extraction using 2-methyl-8-quinolinol.
2003 May 1
Reactivity of aqua coordinated monoporphyrinate lanthanide complexes: synthetic, structural and photoluminescent studies of lanthanide porphyrinate dimers.
2004 Dec 7
Cloud point extraction of iron(III) and vanadium(V) using 8-quinolinol derivatives and Triton X-100 and determination of 10(-7)moldm(-3) level iron(III) in riverine water reference by a graphite furnace atomic absorption spectroscopy.
2005 Jan 30
Blue emitting pentacoordinated Al(III) complexes based on 2-methylquinolin-8-olate and substituted phenolate ligands. The role of phenolate derivatives on emission and absorption properties.
2006 Jan 14
Boxes, helicates, and coordination polymers: a structural and magnetochemical investigation of the diverse coordination chemistry of simple pyridine-alcohol ligands.
2006 Jun 12
[Study on UV-Vis absorption spectra of tetra-azo-aromaticoxy substituted metallophthalocyanines].
2006 Nov
Experimental and computational evidence of the intermolecular motifs in the crystal packing of luminescent pentacoordinated gallium(III) complexes.
2006 Nov 21
Electrogenerated chemiluminescence of the lithium salts of 8-hydroxyquinoline and 2-methyl-8-hydroxyquinoline.
2006 Oct 7
8-Hydroxy-2-methylquinoline.
2007 Dec 6
Synthesis and solid state characterization of hexacoordinated 1:1 ionic gallium(III) complexes.
2008 Mar 7
Bis(μ-2-methyl-quinolin-8-olato)-κN,O:O;κO:N,O-bis-[(acetato-κO)(methanol-κO)zinc(II)].
2009 Apr 22
Bis(μ-2-methyl-quinolin-8-olato)-κN,O:O;κO:N,O-bis-[(methanol-κO)(nitrato-κO,O')lead(II)].
2009 Feb 11
(E)-2-[2-(Penta-fluoro-phen-yl)ethen-yl]-8-quinolyl acetate.
2009 Oct 28
Square structures and photophysical properties of Zn(2)Ln(2) complexes (Ln = Nd, Eu, Sm, Er, Yb).
2010 Feb 28
Chloridometh-yl(2-methyl-quinolin-8-olato-κN,O)phenyl-tin(IV).
2010 Jul 17
8-Hy-droxy-2-methyl-quinolinium dibromido(2-methyl-quinolin-8-olato-κN,O)zincate(II) methanol monosolvate.
2010 Sep 18
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:45:51 GMT 2023
Edited
by admin
on Fri Dec 15 17:45:51 GMT 2023
Record UNII
7W631H5302
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-METHYL-8-HYDROXYQUINOLINE
Systematic Name English
8-QUINOLINOL, 2-METHYL-
Systematic Name English
2-METHYLOXINE
Common Name English
8-HYDROXY-2-METHYLQUINOLINE
Systematic Name English
HYDROXYQUINALDINE
Systematic Name English
2-METHYL-8-QUINOLINOL
Systematic Name English
8-HYDROXYQUINALDINE
Systematic Name English
NSC-58553
Code English
NSC-403349
Code English
HYDROXY-2-METHYLQUINOLINE, 8-
Systematic Name English
Code System Code Type Description
NSC
403349
Created by admin on Fri Dec 15 17:45:51 GMT 2023 , Edited by admin on Fri Dec 15 17:45:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
212-562-6
Created by admin on Fri Dec 15 17:45:51 GMT 2023 , Edited by admin on Fri Dec 15 17:45:51 GMT 2023
PRIMARY
FDA UNII
7W631H5302
Created by admin on Fri Dec 15 17:45:51 GMT 2023 , Edited by admin on Fri Dec 15 17:45:51 GMT 2023
PRIMARY
NSC
58553
Created by admin on Fri Dec 15 17:45:51 GMT 2023 , Edited by admin on Fri Dec 15 17:45:51 GMT 2023
PRIMARY
PUBCHEM
13224
Created by admin on Fri Dec 15 17:45:51 GMT 2023 , Edited by admin on Fri Dec 15 17:45:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID3061184
Created by admin on Fri Dec 15 17:45:51 GMT 2023 , Edited by admin on Fri Dec 15 17:45:51 GMT 2023
PRIMARY
CAS
826-81-3
Created by admin on Fri Dec 15 17:45:51 GMT 2023 , Edited by admin on Fri Dec 15 17:45:51 GMT 2023
PRIMARY