U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C10H10O
Molecular Weight 146.1858
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-TETRALONE

SMILES

O=C1CCCC2=C1C=CC=C2

InChI

InChIKey=XHLHPRDBBAGVEG-UHFFFAOYSA-N
InChI=1S/C10H10O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6H,3,5,7H2

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
The absolute configuration of (+)-isoshinanolone and in situ LC-CD analysis of its stereoisomers from crude extracts.
2001 Feb
Controlled expansion of a molecular cavity in a steroid host compound.
2001 May 16
Stress-related polyketide metabolism of Dioncophyllaceae and Ancistrocladaceae.
2001 Oct
Synthesis of polysubstituted benzothiophenes and sulfur-containing polycyclic aromatic compounds via samarium diiodide promoted three-component coupling reactions of thiophene-2-carboxylate.
2002 Jul 26
Solution structure of a wedge-shaped synthetic molecule at a two-base bulge site in DNA.
2003 Jul 22
Total synthesis of 10-norparvulenone and of O-methylasparvenone using a xanthate-mediated free radical addition-cyclization sequence.
2003 Oct 2
Modification of bitter taste in children.
2003 Sep
BINAP/1,4-diamine-ruthenium(II) complexes for efficient asymmetric hydrogenation of 1-tetralones and analogues.
2004 Aug 5
Effect of 2-(4-aminophenylmethyl)-6-hydroxy-3, 4-dihydronaphthalen-1(2H)-one on all-trans and 13-cis-retinoic acid levels in plasma quantified by high perfomance liquid chromatography coupled to tandem mass spectrometry.
2005 Jun
Studies of the condensation of sulfones with ketones and aldehydes.
2006 Jan 20
Cytotoxic and new tetralone derivatives from Berchemia floribunda (Wall.) Brongn.
2006 Jun
Construction of a chiral central nervous system (CNS)-active aminotetralin drug compound based on a synthesis strategy using multitasking properties of (S)-1-phenylethylamine.
2007 Dec
Oxidative carbon-carbon bond formation via silyl bis-enol ethers: controlled cross-coupling for the synthesis of quaternary centers.
2007 Oct 25
Metabolites from the xylariaceous fungus PSU-A80.
2007 Sep
Two new isomeric alpha-tetralones from Pyrola calliantha.
2008 Dec
In vivo active aldosterone synthase inhibitors with improved selectivity: lead optimization providing a series of pyridine substituted 3,4-dihydro-1H-quinolin-2-one derivatives.
2008 Dec 25
4'-Methyl-3-(4-nitro-phen-yl)-4-phenyl-4,5,1',2',3',4'-hexa-hydro-spiro-[isoxazole-5,2'-naphthalen]-1'-one.
2008 Jan 23
Enantioselective alpha-arylation of ketones with aryl triflates catalyzed by difluorphos complexes of palladium and nickel.
2008 Jan 9
Simultaneous determination of three diarylheptanoids and an alpha-tetralone derivative in the green walnut husks (Juglans regia L.) by high-performance liquid chromatography with photodiode array detector.
2008 May 9
Capillary zone electrophoresis for separation and analysis of four diarylheptanoids and an alpha-tetralone derivative in the green walnut husks (Juglans regia L.).
2008 Nov 4
Facile and efficient enantioselective Strecker reaction of ketimines by chiral sodium phosphate.
2009 Jun 8
4-(4-Fluoro-phen-yl)-2-oxo-1,2,5,6-tetra-hydro-benzo[h]quinoline-3-carbonitrile.
2009 May 20
Diazeniumdiolate mediated nitrosative stress alters nitric oxide homeostasis through intracellular calcium and S-glutathionylation of nitric oxide synthetase.
2010 Nov 30
Patents
Name Type Language
1-TETRALONE
Systematic Name English
TETRALONE
Systematic Name English
1(2H)-NAPHTHALENONE, 3,4-DIHYDRO-
Systematic Name English
.ALPHA.-TETRALONE
Common Name English
3,4-DIHYDRONAPHTHALENONE
Systematic Name English
PHENYLBUTYRATE RELATED COMPOUND B [USP-RS]
Common Name English
NSC-5171
Code English
PHENYLBUTYRATE RELATED COMPOUND B
USP-RS  
Common Name English
Code System Code Type Description
RS_ITEM_NUM
1614556
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
WIKIPEDIA
1-Tetralone
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-460-6
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
NSC
5171
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
PUBCHEM
10724
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
HSDB
5678
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
CAS
529-34-0
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
CAS
29059-07-2
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
NON-SPECIFIC SUBSTITUTION
FDA UNII
6VT52A15HY
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY
EPA CompTox
DTXSID2027175
Created by admin on Fri Dec 15 19:46:35 GMT 2023 , Edited by admin on Fri Dec 15 19:46:35 GMT 2023
PRIMARY