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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H10O2
Molecular Weight 150.1745
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-ACETYLANISOLE

SMILES

COC1=CC=C(C=C1)C(C)=O

InChI

InChIKey=NTPLXRHDUXRPNE-UHFFFAOYSA-N
InChI=1S/C9H10O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-6H,1-2H3

HIDE SMILES / InChI

Molecular Formula C9H10O2
Molecular Weight 150.1745
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Cleavage of nonphenolic beta-1 diarylpropane lignin model dimers by manganese peroxidase from Phanerochaete chrysosporium.
2003 Jan
Preparation of beta- and gamma-lactams from carbamoyl radicals derived from oxime oxalate amides.
2004 Mar 7
Reverse micellar aggregates: effect on ketone reduction. 1. Substrate role.
2004 Nov 26
Time-resolved resonance Raman and density functional theory study of hydrogen-bonding effects on the triplet state of p-methoxyacetophenone.
2005 Apr 21
Substituent effects in the migration step of the Baeyer-Villiger rearrangement. A theoretical study.
2005 Apr 21
Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat 30NP.
2006 Aug 25
Effect of water on the functionalization of substituted anisoles with iodine in the presence of F-TEDA-BF4 or hydrogen peroxide.
2006 Feb 3
Oxygen uptake and involvement of superoxide radicals upon photolysis of ketones in air-saturated aqueous alcohol, formate, amine or ascorbic acid solutions.
2006 May-Jun
Photolabile carboxylic acid protected terpolymers for surface patterning. Part 2: Photocleavage and film patterning.
2006 Oct 24
Photolabile carboxylic acid protected terpolymers for surface patterning. Part 1: Polymer synthesis and film characterization.
2006 Oct 24
Synthesis and physiological activity of thiophenes and furans with 3- and 4-methoxyacetophenone derivatives.
2008
N'-[1-(4-Methoxy-phen-yl)ethyl-idene]acetohydrazide.
2008 Nov 22
2,6-Bis(4-methoxy-phen-yl)-4-phenyl-pyridine.
2009 Dec 4
General methods for flash chromatography using disposable columns.
2009 May
Volatile compounds of flowers and leaves of Sideritis italica (Miller) Greuter et Burdet (Lamiaceae), a plant used as mountain tea.
2010 Apr
Chemical composition of the essential oil of Stachys menthifolia Vis.
2010 Feb
Antioxidant activity and chemical composition of essential oil from Atriplex undulata.
2010 Nov
Photophysics and photodeprotection reactions of p-methoxyphenacyl phototriggers: an ultrafast and nanosecond time-resolved spectroscopic and density functional theory study.
2010 Sep 3
An in vitro test to screen skin sensitizers using a stable THP-1-derived IL-8 reporter cell line, THP-G8.
2011 Dec
Dual regulation of skin sensitizer-induced HMOX1 expression by Bach1 and Nrf2: Comparison to regulation of the AKR1C2-ARE element in the KeratinoSens cell line.
2015 Nov 1
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:52:53 GMT 2023
Edited
by admin
on Fri Dec 15 16:52:53 GMT 2023
Record UNII
0IRH2BR587
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-ACETYLANISOLE
Systematic Name English
NSC-209523
Code English
NSC-5601
Code English
ACETYLANISOLE
Systematic Name English
ACETANISOLE [FCC]
Common Name English
FEMA NO. 2005
Code English
4'-METHOXYACETOPHENONE
Systematic Name English
VANANOTE
Common Name English
LINARODIN
Common Name English
P-ACETYLANISOLE
Common Name English
ACETANISOLE
FCC   FHFI  
Common Name English
4-METHOXY-ACETOPHENONE
Common Name English
NOVATONE
Common Name English
ACETANISOLE [FHFI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION ACETANISOLE
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
Code System Code Type Description
NSC
5601
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
NSC
209523
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
JECFA MONOGRAPH
730
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
CHEBI
86567
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
EVMPD
SUB30345
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
EPA CompTox
DTXSID2044347
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
HSDB
8319
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
RXCUI
2612428
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
PUBCHEM
7476
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
FDA UNII
0IRH2BR587
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
DAILYMED
0IRH2BR587
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
WIKIPEDIA
ACETANISOLE
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
CAS
100-06-1
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
MESH
C046029
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-815-9
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
SMS_ID
100000091012
Created by admin on Fri Dec 15 16:52:53 GMT 2023 , Edited by admin on Fri Dec 15 16:52:53 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE