COUMACHLOR

Details

Stereochemistry	RACEMIC
Molecular Formula	C19H15ClO4
Molecular Weight	342.773
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(=O)CC(C1=CC=C(Cl)C=C1)C2=C(O)C3=C(OC2=O)C=CC=C3

InChI

InChIKey=DEKWZWCFHUABHE-UHFFFAOYSA-N

InChI=1S/C19H15ClO4/c1-11(21)10-15(12-6-8-13(20)9-7-12)17-18(22)14-4-2-3-5-16(14)24-19(17)23/h2-9,15,22H,10H2,1H3

HIDE SMILES / InChI

Molecular Formula	C19H15ClO4
Molecular Weight	342.773
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

PubMed

Title	Date	PubMed
Characterization of warfarin unusual peak profiles on oligoproline chiral high performance liquid chromatography columns.	2010-10-15	20846657
Achiral and chiral separations using MEKC, polyelectrolyte multilayer coatings, and mixed mode separation techniques with molecular micelles.	2010-03	20155738
Separation and determination of warfarin enantiomers in human plasma using a novel polymeric surfactant for micellar electrokinetic chromatography-mass spectrometry.	2007-08-03	17499757
Acute bromadiolone intoxication.	2006-05	16803669
Antihuman Immunodeficiency Virus Type 1 (HIV-1) Activity of Rare Earth Metal Complexes of 4-Hydroxycoumarins in Cell Culture.	2006	17497016
Synthesis, characterization, and cytotoxic activity of new lanthanum(III) complexes of bis-coumarins.	2006	17497005
Use of poly(sodium oleyl-L-leucylvalinate) surfactant for the separation of chiral compounds in micellar electrokinetic chromatography.	2003-09	12973797
Brush-type chiral stationary phase for enantioseparation of acidic compounds. Optimization of chiral capillary electrochromatographic parameters.	2003-07-11	12924792
Toxicology and histopathology of some rodenticides and palatable food items combinations on the common mice Mus musculus var. albus in Egypt.	2003	15151313
Synthesis, physicochemical characterization, and cytotoxic screening of new zirconium complexes with coumarin derivatives.	2001-05	11413821

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:23:04 GMT 2025` Edited by `admin` on `Mon Mar 31 22:23:04 GMT 2025`
Record UNII	UCD8XZW42P
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

EXPERIMENTAL RODENTICIDE 332

Preferred Name

English

COUMACHLOR

Common Name

English

P-CHLOROWARFARIN

Common Name

English

2H-1-BENZOPYRAN-2-ONE, 3-(1-(4-CHLOROPHENYL)-3-OXOBUTYL)-4-HYDROXY-

Systematic Name

English

3-(.ALPHA.-ACETONYL-4-CHLOROBENZYL)-4-HYDROXYCOUMARIN

Systematic Name

English

3-((.ALPHA.-ACETONYL)-4-CHLORBENZYL)-4-HYDROXYCUMARIN [HSDB]

Common Name

English

3-(1-(4-CHLOROPHENYL)-3-OXOBUTYL)-4-HYDROXY-2H-1-BENZOPYRAN-2-ONE

Systematic Name

English

3-(.ALPHA.-ACETONYL-P-CHLOROBENZYL)-4-HYDROXYCOUMARIN

Common Name

English

COUMACHLOR [MI]

Common Name

English

3-(.ALPHA.-ACETONYL-4-CHLOROBENZYL)-4-HYDROXY COUMARIN, (±)-

Systematic Name

English

DL-3-(.ALPHA.-ACETONYL-4-CHLOROBENZYL)-4-HYDROXYCOUMARIN

Common Name

English

P-CHLOROWARFARIN, (±)-

Systematic Name

English

CUMACHLOR

Common Name

English

TOMORIN

Common Name

English

COUMACHLOR, (±)-

Systematic Name

English

3-(1-(4-CHLOROPHENYL)-3-OXOBUTYL)-4-HYDROXYCOUMARIN

Systematic Name

English

3-(.ALPHA.-P-CHLOROPHENYL-.BETA.-ACETYLETHYL)-4-HYDROXYCOUMARIN

Common Name

English

COUMARIN, 3-(.ALPHA.-ACETONYL-P-CHLOROBENZYL)-4-HYDROXY-

Systematic Name

English

3-(1-(P-CHLOROPHENYL)-2-ACETYLETHYL)-4-HYDROXYCOUMARIN

Common Name

English

4-HYDROXY-3-(1-(4-CHLOROPHENYL)-3-OXOBUTYL)-2H-1-BENZOPYRAN-2-ONE

Systematic Name

English

3-(1-ACETYL-2-(P-CHLOROPHENYL)ETHYL)-4-HYDROXYCOUMARIN

Common Name

English

COUMACHLOR [ISO]

Common Name

English

Classification Tree Code System Code

EPA PESTICIDE CODE

224200