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Details

Stereochemistry ACHIRAL
Molecular Formula C12H10O
Molecular Weight 170.2072
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-ACETONAPHTHONE

SMILES

CC(=O)C1=C2C=CC=CC2=CC=C1

InChI

InChIKey=QQLIGMASAVJVON-UHFFFAOYSA-N
InChI=1S/C12H10O/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-8H,1H3

HIDE SMILES / InChI

Molecular Formula C12H10O
Molecular Weight 170.2072
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
(2E)-3-(2-Chloro-6-methyl-3-quinol-yl)-1-(1-naphth-yl)prop-2-en-1-one.
2010-03-06
(E)-3-(4-Chloro-phen-yl)-1-(1-naphth-yl)prop-2-en-1-one.
2009-11-28
Synthesis and antihyperglycemic activity of 2-(substituted phenyl)-3-{[4-(1-naphthyl)-1,3-thiazol-2-yl] amino}-4-oxo-1,3-thiazolidin-5-ylacetic acid derivatives.
2009-02-21
Toxicity, tunneling and feeding behavior of the termite, Coptotermes vastator, in sand treated with oil of the physic nut, Jatropha curcas.
2009
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008-04
Improvement of carbonyl reductase production of Geotrichum candidum for the transformation of 1-acetonaphthone to S(-)-1-(1'-napthyl) ethanol.
2007-07
A ruthenium-catalyzed reaction of aromatic ketones with arylboronates: a new method for the arylation of aromatic compounds via C-H bond cleavage.
2003-02-19
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:50 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:50 GMT 2025
Record UNII
U44R403XVS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-ACETONAPHTHONE
INCI  
INCI  
Official Name English
LIQUID U-80
Preferred Name English
ETHANONE, 1-(1-NAPHTHALENYL)-
Systematic Name English
NSC-7659
Code English
ALPHA-METHYL NAPHTHYL KETONE
Common Name English
1-ACETONAPHTHALENE
Common Name English
Code System Code Type Description
CAS
941-98-0
Created by admin on Mon Mar 31 19:56:50 GMT 2025 , Edited by admin on Mon Mar 31 19:56:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID4052635
Created by admin on Mon Mar 31 19:56:50 GMT 2025 , Edited by admin on Mon Mar 31 19:56:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
213-384-1
Created by admin on Mon Mar 31 19:56:50 GMT 2025 , Edited by admin on Mon Mar 31 19:56:50 GMT 2025
PRIMARY
NSC
7659
Created by admin on Mon Mar 31 19:56:50 GMT 2025 , Edited by admin on Mon Mar 31 19:56:50 GMT 2025
PRIMARY
PUBCHEM
13663
Created by admin on Mon Mar 31 19:56:50 GMT 2025 , Edited by admin on Mon Mar 31 19:56:50 GMT 2025
PRIMARY
FDA UNII
U44R403XVS
Created by admin on Mon Mar 31 19:56:50 GMT 2025 , Edited by admin on Mon Mar 31 19:56:50 GMT 2025
PRIMARY