| Weight | 251.358 g/mol |
|---|---|
| Formula | C12H17NO3Si |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
PHENYLSILATRANE (2097-19-0)
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- Crytal and molecular structures of -1-phenylsilatrane: some structural features of silatranes (Journal of Organometallic Chemistry, 1975)
- Crystal and molecular structure of -1-phenylsilatrane, C12H17NSi (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1974)
- Synthesis and reactivity of (phenylsilatrane)manganese tricarbonyl perchlorate: molecular structure of [{.eta.5-1-N(CH2CH2O)3Si-6-PhC6H5}Mn(CO)3] (Organometallics, 1991)
- Synthesis, characterization, and reactivity of a chromium tricarbonyl complex of phenylsilatrane: molecular structure of [C6H5Si(OCH2CH2)3N]Cr(CO)3 (Organometallics, 1990)
- Preparation and reactivity of (phenylsilatrane)manganese tricarbonyl perchlorate (Organometallics, 1990)
- Synthesis, reactivity, and molecular structure of silatrane manganese complex [(phenylsilatrane)Mn(CO)2P(OMe)3]ClO4 (Organometallics, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CO[Si]2(OCCN1CCO2)C3=CC=CC=C3
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InChIKeyIJOIPPSHQCEBDH-UHFFFAOYSA-N
- Pubchem - PHENYLSILATRANE
- Wikipedia - Phenylsilatrane
Phenylsilatrane is a convulsant chemical which has been used as a rodenticide. Phenylsilatrane and some of its analogs with 4-substituents of H , CH 3 , Cl , Br {\displaystyle {\ce {H, CH3, Cl, Br}}} , and C {\displaystyle {\ce {C}}} CSi ( CH 3 ) 3 {\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.
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