COUMATETRALYL

Details

Stereochemistry	RACEMIC
Molecular Formula	C19H16O3
Molecular Weight	292.3285
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC1=C(C2CCCC3=C2C=CC=C3)C(=O)OC4=C1C=CC=C4

InChI

InChIKey=ULSLJYXHZDTLQK-UHFFFAOYSA-N

InChI=1S/C19H16O3/c20-18-15-9-3-4-11-16(15)22-19(21)17(18)14-10-5-7-12-6-1-2-8-13(12)14/h1-4,6,8-9,11,14,20H,5,7,10H2

HIDE SMILES / InChI

Molecular Formula	C19H16O3
Molecular Weight	292.3285
Charge	0
Count

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

Approval Year

PubMed

Title	Date	PubMed
[Attempted suicide with super warfarin].	2005 Oct	16281750
Acute bromadiolone intoxication.	2006 May	16803669
[Solid phase extraction--HPLC in determination of coumatetralyl in urine].	2006 Nov	17181951
Efficiency of three anti-coagulant rodenticides on commensal rodents.	2007 Aug	17926811
Exposure of raptors and waterbirds to anticoagulant rodenticides (difenacoum, bromadiolone, coumatetralyl, coumafen, brodifacoum): epidemiological survey in Loire Atlantique (France).	2007 Jul	17487436
[Determination of five 4-hydroxycoumarin rodenticides in whole blood by high performance liquid chromatography with fluorescence detection].	2007 Mar	17580689
Identification and determination of coumateralyl and coumafuryl in animal tissues by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry.	2008 Jul	17975848
Multi-residue analysis of eight anticoagulant rodenticides in animal plasma and liver using liquid chromatography combined with heated electrospray ionization tandem mass spectrometry.	2008 Jun 15	18502701
Pharmacokinetics of eight anticoagulant rodenticides in mice after single oral administration.	2008 Oct	19000263
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 Mar	20223102
Thermodynamic and kinetic study of chiral separations of coumarin-based anticoagulants on derivatized amylose stationary phase.	2010 Sep 17	20719321

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 09:38:03 GMT 2023` Edited by `admin` on `Sat Dec 16 09:38:03 GMT 2023`
Record UNII	NWK4HW86A8
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

COUMATETRALYL

Common Name

English

2H-1-BENZOPYRAN-2-ONE, 4-HYDROXY-3-(1,2,3,4-TETRAHYDRO-1- NAPHTHALENYL)-

Systematic Name

English

4-HYDROXY-3-(1,2,3,4-TETRAHYDRO-1-NAPHTHYL)COUMARIN

Systematic Name

English

COUMARIN, 4-HYDROXY-3-(1,2,3,4-TETRAHYDRO-1-NAPHTHYL)-

Systematic Name

English

RACUMIN

Brand Name

English

3-(.ALPHA.-TETRAL)-4-OXYCOUMARIN

Common Name

English

COUMATETRALYL [HSDB]

Common Name

English

3-(.ALPHA.-TETRALYL)-4-HYDROXYCOUMARIN

Common Name

English

4-HYDROXY-3-(1,2,3,4-TETRAHYDRO-1-NAPHTHALENYL)-2H-1- BENZOPYRAN-2-ONE

Systematic Name

English

BAYER 25 634

Brand Name

English

3-(D-TETRALYL)-4-HYDROXYCOUMARIN

Common Name

English

COUMATETRALYL [ISO]

Common Name

English

Classification Tree Code System Code

EPA PESTICIDE CODE

496100