Coumatetralyl

Coumatetralyl
Chemical structure of coumatetralyl
Names
IUPAC name
(RS)-2-Hydroxy-3-(1,2,3,4-tetrahydronaphthalen-1-yl)-4H-chromen-4-one
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.024.931 Edit this at Wikidata
KEGG
UNII
  • 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
  • OC=1c4ccccc4OC(=O)C=1C3CCCc2ccccc23
Properties
C19H16O3
Molar mass 292.334 g·mol−1
Hazards
GHS labelling:
GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard[1]
Danger[1]
H300, H311, H330, H360D, H372, H410[1]
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 ?)

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.).