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Details

Stereochemistry ACHIRAL
Molecular Formula C8H7ClO
Molecular Weight 154.594
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CHLOROACETOPHENONE

SMILES

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

InChI

InChIKey=BUZYGTVTZYSBCU-UHFFFAOYSA-N
InChI=1S/C8H7ClO/c1-6(10)7-2-4-8(9)5-3-7/h2-5H,1H3

HIDE SMILES / InChI

Molecular Formula C8H7ClO
Molecular Weight 154.594
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
(E)-3-(4-Chloro-phen-yl)-3-[3-(4-chloro-phen-yl)-1H-pyrazol-1-yl]prop-2-enal.
2010-09-18
A monoclinic polymorph of 1-(4-chloro-phen-yl)-3-(4-methoxy-phen-yl)prop-2-en-1-one.
2010-01-09
(E)-1-(4-Chloro-phen-yl)-3-[4-(diethyl-amino)phen-yl]prop-2-en-1-one.
2010-01-09
Development of a nanocomposite system by combining an organic dyad 1-(4-chloro-phenyl)-3-(4-methoxy-naphthalen-1-yl)-Propenone with semiconductor TiO2 nanoparticles.
2010-01
(2E)-3-(3-Bromo-phen-yl)-1-(4-chloro-phen-yl)prop-2-en-1-one: a non-merohedral twin.
2009-07-18
(E)-1-(4-Chloro-phen-yl)-3-[4-(dimethyl-amino)phen-yl]prop-2-en-1-one.
2009-03-11
E-[4-(β-d-Allopyranos-yloxy)phen-yl]-1-(4-chloro-phen-yl)prop-2-enone ethanol solvate.
2009-02-28
1,5-Bis(4-chloro-phen-yl)-3-[4-(dimethyl-amino)phen-yl]pentane-1,5-dione.
2009-02-11
(E)-N'-[1-(4-Chloro-phen-yl)ethyl-idene]-2-hydroxy-benzohydrazide.
2009-01-23
N'-[(E)-1-(4-Chloro-phen-yl)ethyl-idene]-2-[4-(2-methyl-prop-yl)phen-yl]propano-hydrazide.
2008-12-03
Asymmetric reduction of prochiral ketones to chiral alcohols catalyzed by plants tissue.
2008-09
(E)-1-(4-Chloro-phen-yl)-3-(4-methyl-phen-yl)prop-2-en-1-one.
2008-05-10
A new facile approach to the synthesis of 3-methylthio-substituted furans, pyrroles, thiophenes, and related derivatives.
2008-05-02
2,4-Bis(4-chloro-benzo-yl)-1-(4-chloro-phen-yl)-3,5-di-2-thienylcyclo-hexa-nol methanol hemisolvate.
2008-04-02
A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides.
2007-05-30
The methoxycarbonylation of aryl chlorides catalysed by palladium complexes of bis(di-tert-butylphosphinomethyl)benzene.
2005-05-21
Bulky triarylarsines are effective ligands for palladium catalysed Heck olefination.
2005-04-21
Oxime carbapalladacycle covalently anchored to high surface area inorganic supports or polymers as heterogeneous green catalysts for the Suzuki reaction in water.
2004-01-23
Ab initio evaluation of intramolecular electron transfer reactions in halobenzenes and stabilized derivatives.
2003-11-28
[Preparation of chiral alcohol by stereoselective reduction of acetophenone and chloroacetophenone with yeast cells].
2003-08
An oxime-carbapalladacycle complex covalently anchored to silica as an active and reusable heterogeneous catalyst for Suzuki cross-coupling in water.
2003-03-07
Electron transfer compatible molecular design of benzothiophene-acetophenone bichromophores: a theoretical approach.
2001-03-01
Cometabolism of 1,1-dichloro-2,2-bis(4-chlorophenyl)ethylene by Pseudomonas acidovorans M3GY grown on biphenyl.
1998-06
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:35:11 GMT 2025
Edited
by admin
on Mon Mar 31 19:35:11 GMT 2025
Record UNII
ZV4A71K303
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-6115
Preferred Name English
P-CHLOROACETOPHENONE
HSDB   MI  
Common Name English
P-CHLOROACETOPHENONE [HSDB]
Common Name English
1-(4-CHLOROPHENYL)ETHANONE
Systematic Name English
4'-CHLOROACETOPHENONE
Systematic Name English
P-CHLOROACETOPHENONE [MI]
Common Name English
ETHANONE, 1-(4-CHLOROPHENYL)-
Systematic Name English
Code System Code Type Description
MERCK INDEX
m3386
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY Merck Index
FDA UNII
ZV4A71K303
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY
PUBCHEM
7467
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY
CAS
99-91-2
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-800-7
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY
NSC
6115
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY
HSDB
2088
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID1052668
Created by admin on Mon Mar 31 19:35:11 GMT 2025 , Edited by admin on Mon Mar 31 19:35:11 GMT 2025
PRIMARY