Cannabis Ruderalis

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Coumachlor
Names
IUPAC name
3-[1-(4-chlorophenyl)-3-oxobutyl]-2-hydroxychromen-4-one
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.001.254 Edit this at Wikidata
UNII
  • 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
    Key: DEKWZWCFHUABHE-UHFFFAOYSA-N
  • InChI=1/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
    Key: DEKWZWCFHUABHE-UHFFFAOYAJ
  • CC(=O)CC(C1=CC=C(C=C1)Cl)C2=C(C3=CC=CC=C3OC2=O)O
Properties
C19H15ClO4
Molar mass 342.77 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Coumachlor is a first generation anticoagulant rodenticide which blocks formation of prothrombin and inhibits blood coagulation causing death by internal haemorrhage.[1][2] The chemical can be absorbed through the skin.[3] The symptoms of human contact can be nosebleeds, bleeding gums, bloody urine, extensive bruising in the absence of injury, fatigue, shortness of breath (dyspnea) on exertion. The human consumption or inhalation of compound can also cause fluid in lungs (pulmonary edema).

References[edit]

  1. ^ http://www.sigmaaldrich.com/catalog/ProductDetail.do?D7=0&N5=SEARCH_CONCAT_PNO%7CBRAND_KEY&N4=189219%7CALDRICH&N25=0&QS=ON&F=SPEC Archived January 19, 2012, at the Wayback Machine
  2. ^ "Archived copy" (PDF). Archived from the original (PDF) on 2012-04-26. Retrieved 2011-12-10.{{cite web}}: CS1 maint: archived copy as title (link)
  3. ^ "Health Content A-Z".
source: https://en.wikipedia.org/wiki/Coumachlor

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