|  | |
| Names | |
|---|---|
| Other names allyl trimethylsilane | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.011.003 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C6H14Si | |
| Molar mass | 114.263 g·mol−1 | 
| Appearance | colorless liquid | 
| Density | 0.719 g/cm3 | 
| Boiling point | 84–88 °C (183–190 °F; 357–361 K) | 
| Hazards | |
| GHS labelling:[1] | |
|   | |
| Warning | |
| H225, H315, H319, H335 | |
| P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, P501 | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Allyltrimethylsilane is the organosilicon compound with the formula (CH3)3SiCH2CH=CH2. The molecule consists of the trimethylsilyl group attached to allyl group. This colorless liquid is used in organic synthesis.[2]
References
- ↑ "Allyltrimethylsilane". pubchem.ncbi.nlm.nih.gov.
- ↑  Hideki Sakurai, Akira Hosomi, Josabro Hayashi (1984). "Conjugate Allylation of α,β-Unsaturated Ketones with Allylsilanes: 4-Phenyl-6-Hepten-2-one". Organic Syntheses. 62: 86. doi:10.15227/orgsyn.062.0086.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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