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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H9NO
Molecular Weight 135.1632
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-AMINOACETOPHENONE

SMILES

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

InChI

InChIKey=GPRYKVSEZCQIHD-UHFFFAOYSA-N
InChI=1S/C8H9NO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,9H2,1H3

HIDE SMILES / InChI

Molecular Formula C8H9NO
Molecular Weight 135.1632
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
1-(4-{[(E)-5-Chloro-2-hy-droxy-benzyl-idene]amino}-phen-yl)ethanone oxime.
2010-09-04
1-(4-{[(E)-4-Methyl-benzyl-idene]amino}-phen-yl)ethanone oxime.
2010-09-04
(E)-1-(4-Amino-phen-yl)-3-(2,4,5-trimeth-oxy-phen-yl)prop-2-en-1-one.
2010-07-10
Novel 6,8-dibromo-4(3H)-quinazolinone derivatives of promising anti-inflammatory and analgesic properties.
2010-04-08
4-Iodo-anilinium perchlorate.
2010-03-20
N'-[1-(4-Amino-phen-yl)ethyl]pyrazine-2-carbohydrazide.
2010-02-06
Sleep loss in resident physicians: the cause of medical errors?
2010
4-({4-[1-(Methoxy-imino)eth-yl]anilino}(phen-yl)methyl-ene)-3-methyl-2-phenyl-1H-pyrazol-5(4H)-one.
2009-11-21
Synthesis and immunomodulatory activites of new 5-hydrazino-3-methyl-4-isothiazolecarboxylic acid ethyl esters.
2009-11-10
Novel 3-(p-substituted phenyl)-6-bromo-4(3H)-quinazolinone derivatives of promising antiinflammatory and analgesic properties.
2009-11-10
(2E)-1-(4-Amino-phen-yl)-3-(2-thien-yl)prop-2-en-1-one ethanol hemisolvate.
2009-09-26
4-[1-(Hydroxy-imino)ethyl]-N-(4-nitro-benzyl-idene)aniline.
2009-09-12
Enzymology of the polyenes pimaricin and candicidin biosynthesis.
2009
(E)-1-(4-Amino-phen-yl)ethanone oxime.
2008-10-22
1-(4-Acetyl-phen-yl)-3-butyrylthio-urea.
2008-07-23
(E)-N'-[1-(4-Amino-phen-yl)ethyl-idene]benzohydrazide.
2008-06-28
Methyl 3-[(E)-1-(4-amino-phen-yl)ethyl-idene]dithio-carbazate.
2008-05-07
Hydrogen bonding in the bromide salts of 4-aminobenzoic acid and 4-aminoacetophenone.
2008-04
TLC-spectrophometric separation and trace determination of monocrotophos and dichlorvos in enviromental and biological samples.
2007-04
[DBPs formation characteristics in chlorinating and relationship with chemical structure of some aromatic organic matter].
2006-08
Schiff bases of gossypol: an NMR and DFT study.
2005-04
Synthesis and pharmaceutical activity of new series of chromonyl derivatives.
2004-04-17
Synthesis of novel dihydropyridine, dihydropyrimidine, dithioacetal and chalcone derivatives from formylchromones.
2004-03
Biodegradation of nonylphenol in river sediment.
2004
Determination of thiopurine methyltransferase phenotype in isolated human erythrocytes using a new simple nonradioactive HPLC method.
2003-10
Synthesis of new 2-thiouracil-5-sulfonamide derivatives with biological activity.
2002-06
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:31:44 GMT 2025
Edited
by admin
on Mon Mar 31 19:31:44 GMT 2025
Record UNII
1S58KH902I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-ACETYLANILINE
HSDB  
Preferred Name English
4-AMINOACETOPHENONE
Common Name English
NSC-3242
Code English
4-ACETYLANILINE [HSDB]
Common Name English
1-(4-aminophenyl)ethanone
Systematic Name English
CLENBUTEROL HYDROCHLORIDE IMPURITY D [EP IMPURITY]
Common Name English
Code System Code Type Description
CAS
99-92-3
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
HSDB
2711
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
PUBCHEM
7468
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
MESH
C032065
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
FDA UNII
1S58KH902I
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID6052669
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-801-2
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
NSC
3242
Created by admin on Mon Mar 31 19:31:44 GMT 2025 , Edited by admin on Mon Mar 31 19:31:44 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY