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Phenylsilatrane
| Stereo structural formula of phenylsilatrane | ||
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Preferred IUPAC name
Phenylsilatrane | |
|---|---|---|
| Systematic IUPAC name
1-Phenyl-2,8,9-trioxa-5λ5-aza-1-silatricyclo[3.3.3.01,5]undecan-5-ylium-1-uide | ||
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2097-19-0 7px[[Category:Articles with changed CASNo identifier#REDIRECTmw:Help:Magic words#Other This page is a soft redirect.?]] | |
| ChemSpider | 4321483 7px | |
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| Jmol-3D images | Image | |
| PubChem | Template:Chembox PubChem/format | |
| colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other This page is a soft redirect. Properties #REDIRECTmw:Help:Magic words#Other |
C12H17NO3Si | |
| Molar mass | Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1 | |
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Main hazards | Toxic |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | ||
| Infobox references | ||
Phenylsilatrane is a convulsant chemical which has been used as a rodenticide.[1][2][3]
See also
References
- ^ Voronkov, M. G. (1966). "Silatranes: Intra-Complex Heterocyclic Compounds of Pentacoordinated Silicon" (PDF). Pure and Applied Chemistry 13 (1–2): 35–60. doi:10.1351/pac196613010035.
- ^ Lukevics, E.; Ignatovich, L.; Khokhlova, L.; Belyakov, S. (1997). "Synthesis, Structure, and Toxicity of Arylgermatranes". Chemistry of Heterocyclic Compounds 33 (2): 239–241. doi:10.1007/BF02256767.
- ^ Horsham, M. A.; Palmer, C. J.; Cole, L. M.; Casida, J. E. (1990). "4-Alkynylphenylsilatranes: Insecticidal Activity, Mammalian Toxicity, and Mode of Action". Journal of Agricultural and Food Chemistry 38 (8): 1734–1738. doi:10.1021/jf00098a023.
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