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Details

Stereochemistry ACHIRAL
Molecular Formula C9H10O
Molecular Weight 134.1751
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-METHYL ACETOPHENONE

SMILES

CC(=O)C1=CC=C(C)C=C1

InChI

InChIKey=GNKZMNRKLCTJAY-UHFFFAOYSA-N
InChI=1S/C9H10O/c1-7-3-5-9(6-4-7)8(2)10/h3-6H,1-2H3

HIDE SMILES / InChI

Molecular Formula C9H10O
Molecular Weight 134.1751
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Keto-enol/enolate equilibria in the N-acetylamino-p-methylacetophenone system. Effect of a beta-nitrogen substituent.
2001 Sep 19
Development of new synthetic methods with aryl 1-chlorovinyl sulfoxides.
2004
Antioxidant activity of plant extracts on the inhibition of citral off-odor formation.
2004 Sep
Formation mechanism of p-methylacetophenone from citral via a tert-alkoxy radical intermediate.
2004 Sep 8
In vitro effects of essential oils from Ostericum koreanum against antibiotic-resistant Salmonella spp.
2005 Jul
Combined ruthenium(II) and lipase catalysis for efficient dynamic kinetic resolution of secondary alcohols. Insight into the racemization mechanism.
2005 Jun 22
Potent inhibitory effects of black tea theaflavins on off-odor formation from citral.
2006 Apr 19
Comprehensive two-dimensional gas chromatographic analysis of commercial lemon-flavored beverages.
2006 Oct
Liquid-chromatographic separation and determination of process-related impurities, including a regio-specific isomer of celecoxib on reversed-phase C18 column dynamically coated with hexamethyldisilazane.
2006 Sep
(2E)-1-(4-Methyl-phen-yl)-3-(2,3,5-trichloro-phen-yl)prop-2-en-1-one.
2007 Dec 6
Synthesis and in vivo evaluation of [18F]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide as a PET imaging probe for COX-2 expression.
2007 Feb 15
Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.
2008 Jul 23
1,3,5-Tri-p-tolyl-pentane-1,5-dione.
2008 Nov 13
(E)-3-(4-Methyl-phen-yl)-3-[3-(4-methyl-phen-yl)-1H-pyrazol-1-yl]-2-propenal.
2008 Oct 31
(E)-3-(3-Bromo-phen-yl)-1-(4-methyl-phenyl)prop-2-en-1-one.
2008 Oct 31
Site-isolation and recycling of PdCl(2) using PDMS thimbles.
2009 Jul 3
N-(2,4-Dinitro-phen-yl)-N'-(1-p-tolyl-ethyl-idene)hydrazine.
2009 Mar 25
Synthesis, spectral, thermal and anti-fungal studies of organotin(IV) thiohydrazone complexes.
2009 May
4-Phenyl-2,6-bis-(4-tol-yl)pyridine.
2010 Aug 18
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:37 GMT 2023
Edited
by admin
on Fri Dec 15 15:02:37 GMT 2023
Record UNII
AX66V0KX3Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-METHYL ACETOPHENONE
INCI  
INCI  
Official Name English
4-METHYLPHENYL METHYL KETONE
Systematic Name English
METHYLACETOPHENONE
Systematic Name English
METHYL-P-TOLYL KETONE
Common Name English
NSC-9401
Code English
P-METHYLACETOPHENONE
Common Name English
4-METHYL ACETOPHENONE
FCC  
Common Name English
4-METHYLACETOPHENONE
Common Name English
P-METHYL ACETOPHENONE [INCI]
Common Name English
4'-METHYLACETOPHENONE [FHFI]
Common Name English
P- METHYLACETOPHENONE
Common Name English
4'-METHYLACETOPHENONE
FHFI  
Systematic Name English
4-METHYL ACETOPHENONE [FCC]
Common Name English
MELILOTAL
Common Name English
FEMA NO. 2677
Code English
ACETOPHENONE, 4'-METHYL-
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION 4-METHYLACETOPHENONE
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
Code System Code Type Description
RS_ITEM_NUM
1A00900
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
PRIMARY
FDA UNII
AX66V0KX3Y
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
PRIMARY
JECFA MONOGRAPH
787
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
PRIMARY
SMS_ID
100000174529
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
PRIMARY
CAS
122-00-9
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
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NSC
9401
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
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PUBCHEM
8500
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID9044374
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-514-8
Created by admin on Fri Dec 15 15:02:37 GMT 2023 , Edited by admin on Fri Dec 15 15:02:37 GMT 2023
PRIMARY