Phenylsilatrane

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Phenylsilatrane

Preferred IUPAC name Phenylsilatrane
Systematic name 1-Phenyl-2,8,9-trioxa-5λ⁵-aza-1-silatricyclo[3.3.3.0^1,5]undecan-5-ylium-1-uide
Identifiers
CAS number	2097-19-0 ^Y
PubChem	5147995
ChemSpider	4321483^Y
Jmol-3D images	{{#if:C1C[N+]23CCO[Si-]2(O1)(OCC3)C1=CC=CC=C1\|Image 1
SMILES C1C[N+]23CCO[Si-]2(O1)(OCC3)C1=CC=CC=C1
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
Properties
Molecular formula	C₁₂H₁₇NO₃Si
Molar mass	251.35 g mol⁻¹
Hazards
Main hazards	Toxic
Except where noted otherwise, 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]

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.

1st generation	Warfarin Coumatetralyl

2nd generation	Brodifacoum Bromadiolone Difenacoum Flocoumafen

Others

Organochlorine

Organophosphorus

Others

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