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# Phenylsilatrane

Names Identifiers 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 CAS Number 3D model (JSmol) ChemSpider ECHA InfoCard 100.016.603 PubChem CID InChI InChI=1S/C12H17NO3Si/c1-2-4-12(5-3-1)17-13(6-9-14-17,7-10-15-17)8-11-16-17/h1-5H,6-11H2 Key: LDOWJVBCZRHOKX-UHFFFAOYSA-N SMILES C1C[N+]23CCO[Si-]2(O1)(OCC3)C1=CC=CC=C1 Chemical formula C12H17NO3Si Molar mass 251.36 g·mol−1 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] Phenylsilatrane and some of its analogs with 4-substituents of ${\displaystyle {\ce {H, CH3, Cl, Br}}}$, and ${\displaystyle {\ce {C}}}$ ${\displaystyle {{\ce {CSi(CH3)3}}}}$ are highly toxic to mice. They have been observed in the laboratory to inhibit the (35)S-tert-butylbicyclophosphorothionate or TBPS binding site (GABA-gated chloride channel) of mouse brain membranes.[3]

## References

1. ^ 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.
2. ^ 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.
3. ^ 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.