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Names | |
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Preferred IUPAC name
1-{3-[3,5-Bis(trifluoromethyl)phenyl]prop-2-yn-1-yl}-4-tert-butylpiperidine | |
Identifiers | |
3D model (
JSmol)
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ChemSpider | |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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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).
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Flupropadine is a rodenticide. [1] [2] Originally made by May and Baker [3] and tested on farms in the United Kingdom it was withdrawn from use by 1994. [4] Flupropadine has a delayed action, and so rodents can have multiple feeds from the bait before being killed. [5]
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. [6]
![]() | |
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 | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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. [1] [2] Originally made by May and Baker [3] and tested on farms in the United Kingdom it was withdrawn from use by 1994. [4] Flupropadine has a delayed action, and so rodents can have multiple feeds from the bait before being killed. [5]
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. [6]