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Fumarin

From Wikipedia, the free encyclopedia

Fumarin
Names
IUPAC name
3-[1-(2-furyl)-3-oxobutyl]-2-hydroxy-4-chromenone
Other names
Coumafuryl, Ratafin, Fumarine
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.003.814 Edit this at Wikidata
EC Number
  • 204-195-5
KEGG
UNII
  • InChI=1S/C17H14O5/c1-10(18)9-12(13-7-4-8-21-13)15-16(19)11-5-2-3-6-14(11)22-17(15)20/h2-8,12,19H,9H2,1H3 checkY
    Key: JFIXKFSJCQNGEK-UHFFFAOYSA-N checkY
  • CC(=O)CC(c1ccco1)c2c(c3ccccc3oc2=O)O
Properties[1]
C17H14O5
Molar mass 298.29 g/mol
Density 1.36 g/cm3
Melting point 124
538 mg/L [20 °C]
log P 1.6
Hazards
Flash point 214.2 °C (417.6 °F; 487.3 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Fumarin, also known as coumafuryl is a coumarin derivative, a structural analog of warfarin. It can be used as rodenticide.[2][3][4]

YouTube Encyclopedic

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  • Inês silva aprende a fumar! In Magalluf
  • Dejar de fumar / Rauchen aufzuhören - Bert Hellinger

Transcription

References

  1. ^ Pesticide Properties Database. "Coumafuryl". University of Hertfordshire.
  2. ^ Sato, Shouichi (2005). "Coumarin rodenticides". Drugs and Poisons in Humans. pp. 599–608. doi:10.1007/3-540-27579-7_66. ISBN 3540222774.
  3. ^ Jin, Mi‐Cong; Xu, Guo‐Zhang; Ren, Yi‐Ping; Chen, Xiao‐Hong; Xu, Xiao‐Ming (2008). "Identification and determination of coumateralyl and coumafuryl in animal tissues by high‐performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry". Journal of Applied Toxicology. 28 (5): 621–627. doi:10.1002/jat.1313. PMID 17975848. S2CID 25178142.
  4. ^ "Compendium of Pesticide Common Names". BCPC.
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This page was last edited on 8 February 2023, at 20:19
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