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Details

Stereochemistry RACEMIC
Molecular Formula C23H15ClO3
Molecular Weight 374.816
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLOROPHACINONE

SMILES

ClC1=CC=C(C=C1)C(C(=O)C2C(=O)C3=CC=CC=C3C2=O)C4=CC=CC=C4

InChI

InChIKey=UDHXJZHVNHGCEC-UHFFFAOYSA-N
InChI=1S/C23H15ClO3/c24-16-12-10-15(11-13-16)19(14-6-2-1-3-7-14)23(27)20-21(25)17-8-4-5-9-18(17)22(20)26/h1-13,19-20H

HIDE SMILES / InChI

Molecular Formula C23H15ClO3
Molecular Weight 374.816
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
A high-throughput screen for teratogens using human pluripotent stem cells.
2014-01
Warfarin toxicity and individual variability-clinical case.
2010-11
Prevalence of anticoagulant rodenticide poisoning in humans and animals in France and substances involved.
2010-11
[Rapid qualitative analysis of indandione rodenticides by high-performance liquid chromatography coupled with ion trap mass spectrometry].
2010-09
Validation of a new liquid chromatography- tandem mass spectrometry ion-trap technique for the simultaneous determination of thirteen anticoagulant rodenticides, drugs, or natural products.
2010-03
[Simultaneous determination of trace diphacinone and chlorophacinone in biological samples by high performance liquid chromatography coupled with ion trap mass spectrometry].
2010-02
Anticoagulant rodenticides in three owl species from Western Canada, 1988-2003.
2010-02
Possible interaction between a rodenticide treatment and a pathogen in common vole (Microtus arvalis) during a population peak.
2009-12-20
Consequences of the Y139F Vkorc1 mutation on resistance to AVKs: in-vivo investigation in a 7th generation of congenic Y139F strain of rats.
2009-10
Potentiometric determination of ionisation constants for diphacinone and chlorophacinone in a dioxane-water cosolvent system.
2009-08-15
Simultaneous measurement of indandione-type rodenticides in human serum by liquid chromatography-electrospray ionization- tandem mass spectrometry.
2009-08-06
Characterization and determination of chlorophacinone in plasma by ion chromatography coupled with ion trap electrospray ionization mass spectrometry.
2009-05
Analysis of indandione anticoagulant rodenticides in animal liver by eluent generator reagent free ion chromatography coupled with electrospray mass spectrometry.
2008-12-05
Pharmacokinetics of eight anticoagulant rodenticides in mice after single oral administration.
2008-10
Lesions associated with the plexus venosus subcutaneus collaris of pigeons with chlorophacinone toxicosis.
2008-09
Multi-residue analysis of eight anticoagulant rodenticides in animal plasma and liver using liquid chromatography combined with heated electrospray ionization tandem mass spectrometry.
2008-06-15
Case of the month: "Oh! Drat!--A case of transcutaneous superwarfarin poisoning and its recurrent presentation".
2007-04
Lethal paradoxical cerebral vein thrombosis due to suspicious anticoagulant rodenticide intoxication with chlorophacinone.
2007-03-02
Multiresidue analysis of seven anticoagulant rodenticides by high-performance liquid chromatography/electrospray/mass spectrometry.
2007-02-07
Chlorophacinone exposure causing an epizootic of acute fatal hemorrhage in lambs.
2006-09
Development of a cell culture/ELISA assay to detect anticoagulant rodenticides and its application to analysis of rodenticide treated grain.
2006-03-08
Assessment of ruminal degradation, oral bioavailability, and toxic effects of anticoagulant rodenticides in sheep.
2006-02
The genetic basis of resistance to anticoagulants in rodents.
2005-08
Anticoagulant rodenticides.
2005
Evidence of secondary poisoning of free-ranging riparian mustelids by anticoagulant rodenticides in France: implications for conservation of European mink (Mustela lutreola).
2004-10
Toxicology and histopathology of some rodenticides and palatable food items combinations on the common mice Mus musculus var. albus in Egypt.
2003
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:39:42 GMT 2025
Edited
by admin
on Mon Mar 31 19:39:42 GMT 2025
Record UNII
34Y6E0063Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MURIOL
Preferred Name English
CHLOROPHACINONE
HSDB   ISO   MART.   MI  
Common Name English
CHLORFACINON
Common Name English
CHLOROPHACINONE [MI]
Common Name English
CHLOROPHACINONE [ISO]
Common Name English
CHLOROPHACINONE [MART.]
Common Name English
ROZOL
Common Name English
LIPHADIONE
Common Name English
RAMUCIDE
Brand Name English
CHLOROPHACINONE [HSDB]
Common Name English
2-(2-(4-CHLOROPHENYL)-2-PHENYLACETYL)INDAN-1, 3-DIONE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 67707
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
Code System Code Type Description
PUBCHEM
19402
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
FDA UNII
34Y6E0063Y
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
ALANWOOD
chlorophacinone
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
HSDB
6432
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
SMS_ID
300000053213
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
WIKIPEDIA
CHLOROPHACINONE
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
CAS
3691-35-8
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
MESH
C004662
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
MERCK INDEX
m3425
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
223-003-0
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID2032348
Created by admin on Mon Mar 31 19:39:42 GMT 2025 , Edited by admin on Mon Mar 31 19:39:42 GMT 2025
PRIMARY