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
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.
2015-11-01
An in vitro test to screen skin sensitizers using a stable THP-1-derived IL-8 reporter cell line, THP-G8.
2011-12
Antioxidant activity and chemical composition of essential oil from Atriplex undulata.
2010-11
Synthesis, Characterization, and Biological Evaluation of certain 6-methyl-2(3H)-benzo-1, 3-thiazolyl-1'-ethylidene-2-(o, p- Substituted Acetophenones) Hydrazine Analogs.
2010-10
Triphen-yl[(4-phenyl-benzo-yl)meth-yl]phospho-nium trifluoro-methane-sulfonate.
2010-09-30
Photophysics and photodeprotection reactions of p-methoxyphenacyl phototriggers: an ultrafast and nanosecond time-resolved spectroscopic and density functional theory study.
2010-09-03
(E)-3-(3-Chloro-phen-yl)-1-(4-methoxy-phen-yl)prop-2-en-1-one.
2010-05-15
Volatile compounds of flowers and leaves of Sideritis italica (Miller) Greuter et Burdet (Lamiaceae), a plant used as mountain tea.
2010-04
Synthesis and biological screening of a combinatorial library of beta-chlorovinyl chalcones as anticancer, anti-inflammatory and antimicrobial agents.
2010-03-01
Chemical composition of the essential oil of Stachys menthifolia Vis.
2010-02
2,6-Bis(4-methoxy-phen-yl)-4-phenyl-pyridine.
2009-12-04
Using a water-immiscible ionic liquid to improve asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one catalyzed by immobilized Candida parapsilosis CCTCC M203011 cells.
2009-10-22
(Z)-3-(9-Anthr-yl)-1-(4-methoxy-phen-yl)prop-2-en-1-one.
2009-10-10
Efficient enantioselective reduction of 4'-methoxyacetophenone with immobilized Rhodotorula sp. AS2.2241 cells in a hydrophilic ionic liquid-containing co-solvent system.
2009-09-10
2-Bromo-1-(4-methoxy-phen-yl)ethanone.
2009-08-26
(E)-3-(2,6-Dichloro-phen-yl)-1-(4-methoxy-phen-yl)prop-2-en-1-one.
2009-06-06
General methods for flash chromatography using disposable columns.
2009-05
N'-[1-(4-Methoxy-phen-yl)ethyl-idene]acetohydrazide.
2008-11-22
Synthesis and physiological activity of thiophenes and furans with 3- and 4-methoxyacetophenone derivatives.
2008
Photolabile carboxylic acid protected terpolymers for surface patterning. Part 2: Photocleavage and film patterning.
2006-10-24
Photolabile carboxylic acid protected terpolymers for surface patterning. Part 1: Polymer synthesis and film characterization.
2006-10-24
Hydrogenation of aromatic ketones, aldehydes, and epoxides with hydrogen and Pd(0)EnCat 30NP.
2006-08-25
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
Effect of water on the functionalization of substituted anisoles with iodine in the presence of F-TEDA-BF4 or hydrogen peroxide.
2006-02-03
Time-resolved resonance Raman and density functional theory study of hydrogen-bonding effects on the triplet state of p-methoxyacetophenone.
2005-04-21
Substituent effects in the migration step of the Baeyer-Villiger rearrangement. A theoretical study.
2005-04-21
Reverse micellar aggregates: effect on ketone reduction. 1. Substrate role.
2004-11-26
Preparation of beta- and gamma-lactams from carbamoyl radicals derived from oxime oxalate amides.
2004-03-07
Cleavage of nonphenolic beta-1 diarylpropane lignin model dimers by manganese peroxidase from Phanerochaete chrysosporium.
2003-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:37:26 GMT 2025
Edited
by admin
on Mon Mar 31 18:37:26 GMT 2025
Record UNII
0IRH2BR587
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-ACETYLANISOLE
Systematic Name English
ACETANISOLE
FCC   FHFI  
Preferred 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-METHOXYACETOPHENONE
Common Name English
P-ACETYLANISOLE
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 Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
Code System Code Type Description
NSC
5601
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
NSC
209523
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
JECFA MONOGRAPH
730
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
CHEBI
86567
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
EVMPD
SUB30345
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID2044347
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
HSDB
8319
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
RXCUI
2612428
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
PUBCHEM
7476
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
FDA UNII
0IRH2BR587
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
DAILYMED
0IRH2BR587
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
WIKIPEDIA
ACETANISOLE
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
CAS
100-06-1
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
MESH
C046029
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-815-9
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
SMS_ID
100000091012
Created by admin on Mon Mar 31 18:37:26 GMT 2025 , Edited by admin on Mon Mar 31 18:37:26 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> METABOLITE