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
Preparation of beta- and gamma-lactams from carbamoyl radicals derived from oxime oxalate amides.
2004 Mar 7
Photolabile carboxylic acid protected terpolymers for surface patterning. Part 2: Photocleavage and film patterning.
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
(E)-3-(2,6-Dichloro-phen-yl)-1-(4-methoxy-phen-yl)prop-2-en-1-one.
2009 Jun 6
General methods for flash chromatography using disposable columns.
2009 May
(Z)-3-(9-Anthr-yl)-1-(4-methoxy-phen-yl)prop-2-en-1-one.
2009 Oct 10
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 Oct 22
Efficient enantioselective reduction of 4'-methoxyacetophenone with immobilized Rhodotorula sp. AS2.2241 cells in a hydrophilic ionic liquid-containing co-solvent system.
2009 Sep 10
(E)-3-(3-Chloro-phen-yl)-1-(4-methoxy-phen-yl)prop-2-en-1-one.
2010 May 15
Antioxidant activity and chemical composition of essential oil from Atriplex undulata.
2010 Nov
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 Oct
Photophysics and photodeprotection reactions of p-methoxyphenacyl phototriggers: an ultrafast and nanosecond time-resolved spectroscopic and density functional theory study.
2010 Sep 3
Triphen-yl[(4-phenyl-benzo-yl)meth-yl]phospho-nium trifluoro-methane-sulfonate.
2010 Sep 30
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