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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 2-ACETONAPHTHONE

SMILES

CC(=O)C1=CC2=C(C=CC=C2)C=C1

InChI

InChIKey=XSAYZAUNJMRRIR-UHFFFAOYSA-N
InChI=1S/C12H10O/c1-9(13)11-7-6-10-4-2-3-5-12(10)8-11/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
Toxicity and inhibition of feeding and tunneling response of naphthalene and 10 derivatives on the formosan subterranean termite (Isoptera: Rhinotermitidae).
2010-12
Synthesis, anticonvulsant and antimicrobial activities of some new 2-acetylnaphthalene derivatives.
2010-04-15
1-(2-Naphth-yl)-3-phenyl-prop-2-en-1-one.
2009-07-04
Facile and efficient enantioselective Strecker reaction of ketimines by chiral sodium phosphate.
2009-06-08
Supra-nanosecond dynamics of a red-to-blue photon upconversion system.
2009-03-16
[The triplet properties of beta-carotene in acetonitrile solution: a laser flash photolysis study].
2008-03
On the effect of 1,4-diazabicyclo[2.2.2]octane on the singlet-oxygen dimol emission: photosensitized generation of (1O2)2.
2007-05-24
Aqueous oxidation of phenylurea herbicides by triplet aromatic ketones.
2006-11-01
Gas chromatography-microchip atmospheric pressure chemical ionization-mass spectrometry.
2006-05-01
Oxygen uptake and involvement of superoxide radicals upon photolysis of ketones in air-saturated aqueous alcohol, formate, amine or ascorbic acid solutions.
2006-03-02
Binding properties of 2-acetylnaphthalene with hydroxypropyl cyclodextrins from fluorescence quenching experiments.
2005-05
Environmental photodegradation of mefenamic acid.
2005-03
Rapid detection and characterization of minor reactive metabolites using stable-isotope trapping in combination with tandem mass spectrometry.
2005
Survivorship, tunneling and feeding behaviors of Coptotermes formosanus (Isoptera: Rhinotermitidae) in response to 2'-acetonaphthone-treated sand.
2004-08
Probing the binding dynamics to sodium cholate aggregates using naphthalene derivatives as guests.
2003-11
Synthesis and anticonvulsant activity of some new dioxolane derivatives.
2003
Patents
Substance Class Chemical
Created
by admin
on Wed Apr 02 18:41:10 GMT 2025
Edited
by admin
on Wed Apr 02 18:41:10 GMT 2025
Record UNII
21D49LOP2T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHYL .BETA.-NAPHTHYL KETONE
FHFI  
Preferred Name English
2-ACETONAPHTHONE
INCI  
INCI  
Official Name English
BETA.-ACETYLNAPHTHALENE
Common Name English
2-NAPHTHYL METHYL KETONE
Systematic Name English
BETA.-NAPHTHYL METHYL KETONE
Common Name English
METHYL .BETA.-NAPHTHYL KETONE [FHFI]
Common Name English
2'-ACETONAPHTHONE
Systematic Name English
1-(2-NAPHTHALENYL)ETHANONE
Systematic Name English
METHYL BETA-NAPHTHYL KETONE
FCC  
Systematic Name English
METHYL 2-NAPHTHYL KETONE
Systematic Name English
2-ACETYLNAPHTHALENE
Systematic Name English
METHYL BETA-NAPHTHYL KETONE [FCC]
Common Name English
1-(2-NAPHTHYL)ETHANONE
Systematic Name English
1-(NAPHTHALEN-3-YL)ETHANONE
Systematic Name English
ETHANONE, 1-(2-NAPHTHALENYL)-
Systematic Name English
.BETA.-ACETONAPHTHONE
Common Name English
1-(NAPHTHALEN-2-YL)ETHANONE
Systematic Name English
NSC-7658
Code English
FEMA NO. 2723
Code English
Classification Tree Code System Code
JECFA EVALUATION METHYL BETA-NAPHTHYL KETONE
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
CFR 21 CFR 172.515
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
JECFA EVALUATION METHYL BETA-NAPHTHYL KETONE
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
Code System Code Type Description
CAS
93-08-3
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-216-2
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
MESH
C503376
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID2041389
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
RXCUI
2378835
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
DAILYMED
21D49LOP2T
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
NSC
7658
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
CHEBI
52364
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
FDA UNII
21D49LOP2T
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
JECFA MONOGRAPH
797
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY
PUBCHEM
7122
Created by admin on Wed Apr 02 18:41:11 GMT 2025 , Edited by admin on Wed Apr 02 18:41:11 GMT 2025
PRIMARY