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Flupropadine
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    Flupropadine

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    Flupropadine
    Flupropadine.svg
    Names
    Preferred IUPAC name
    1-{3-[3,5-Bis(trifluoromethyl)phenyl]prop-2-yn-1-yl}-4-tert-butylpiperidine
    Identifiers
    3D model (JSmol)
    ChemSpider
    PubChem CID
    UNII
    • InChI=1S/C20H23F6N/c1-18(2,3)15-6-9-27(10-7-15)8-4-5-14-11-16(19(21,22)23)13-17(12-14)20(24,25)26/h11-13,15H,6-10H2,1-3H3
      Key: KCVJZJNNTBOLKH-UHFFFAOYSA-N
    • CC(C)(C)C1CCN(CC1)CC#Cc2cc(cc(c2)C(F)(F)F)C(F)(F)F
    Properties
    C20H23F6N
    Molar mass 391.401 g·mol−1
    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    Flupropadine is a rodenticide. Originally made by May and Baker and tested on farms in the United Kingdom it was withdrawn from use by 1994. Flupropadine has a delayed action, and so rodents can have multiple feeds from the bait before being killed.

    The molecule has two rings, one is a m-hexafluoroxylene, and the other is piperidine. Flupropadine is made from 3,5-bis(trifluoromethyl)iodobenzene, propargyl alcohol, and 4-tert-butylpiperidine.


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