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Coumatetralyl information


Coumatetralyl
Chemical structure of coumatetralyl
Names
IUPAC name
(RS)-2-Hydroxy-3-(1,2,3,4-tetrahydronaphthalen-1-yl)-4H-chromen-4-one
Identifiers
CAS Number
  • 5836-29-3 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 10468736 checkY
ECHA InfoCard 100.024.931 Edit this at Wikidata
KEGG
  • C16806 checkY
PubChem CID
  • 54678504
UNII
  • NWK4HW86A8 checkY
CompTox Dashboard (EPA)
  • DTXSID8041799 Edit this at Wikidata
InChI
  • 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 checkY
    Key: ULSLJYXHZDTLQK-UHFFFAOYSA-N checkY
  • InChI=1/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
    Key: ULSLJYXHZDTLQK-UHFFFAOYAA
SMILES
  • OC=1c4ccccc4OC(=O)C=1C3CCCc2ccccc23
Properties
Chemical formula
 C19H16O3
Molar mass 292.334 g·mol−1
Hazards
GHS labelling:
Pictograms
 GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard[1]
Signal word
 Danger[1]
Hazard statements
 H300, H311, H330, H360D, H372, H410[1]
Precautionary statements
 P201, P202, P260, P264, P270, P271, P273, P280, P281, P284, P301+P310, P302+P352, P304+P340, P308+P313, P310, P312, P314, P320, P321, P322, P330, P361, P363, P391, P403+P233, P405, P501[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Coumatetralyl is an anticoagulant of the 4-hydroxycoumarin vitamin K antagonist type used as a rodenticide.[2]

  1. ^ a b c d "Coumatetralyl". PubChem. National Center for Biotechnology Information. Retrieved 2021-11-25.
  2. ^ J. Routt Reigart and James R. Roberts, ed. (2013). "Chapter 18: Rodenticides". Recognition and Management of Pesticide Poisonings (PDF) (6th ed.).

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Coumatetralyl

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Coumatetralyl is an anticoagulant of the 4-hydroxycoumarin vitamin K antagonist type used as a rodenticide. Coumatetralyl is commonly used with grains...

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Rodenticide

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Class Examples Coumarins/4-hydroxycoumarins First generation: warfarin, coumatetralyl Second generation: difenacoum, brodifacoum, flocoumafen and bromadiolone...

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1080 usage in New Zealand

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poison currently available in New Zealand. Pindone, diphacinone, and coumatetralyl are the first-generation anticoagulants most commonly used for pest...

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Warfarin

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around the world. Other 4-hydroxycoumarins used as rodenticides include coumatetralyl and brodifacoum, which is sometimes referred to as "super-warfarin"...

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Phytomenadione

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including warfarin overdose (also overdose of similar compounds such as coumatetralyl), vitamin K deficiency, and obstructive jaundice. It is used to prevent...

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Vitamin K antagonist

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rodenticides, see the main article on 4-hydroxycoumarins. Warfarin (Coumadin) Coumatetralyl Phenprocoumon Acenocoumarol Dicoumarol Tioclomarol Brodifacoum Another...

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Australian boobook

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second-generation anticoagulant rat poison. Older poisons such as warfarin or coumatetralyl were unlikely to affect owls. BirdLife International (2016). "Ninox...

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C19H16O3

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1099 u) may refer to: 1,7-Bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one Coumatetralyl This set index page lists chemical structure articles associated with...

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Index of pesticide articles

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pesticide Copper(I) cyanide Copper(II) arsenate Copper(II) sulfate Coumatetralyl Crimidine Cycloheximide Cyhalothrin Cyromazine Davicil DCMU DDT DDT...

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