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Vinylsilane information


Vinylsilane
Names
Preferred IUPAC name
Ethenylsilane
Other names
Vinyl silane
Identifiers
CAS Number
  • 7291-09-0 checkY
ECHA InfoCard 100.027.926 Edit this at Wikidata
PubChem CID
  • 81714
UNII
  • J8E4H47LQC checkY
CompTox Dashboard (EPA)
  • DTXSID10894876 Edit this at Wikidata
Properties
Chemical formula
C2H6Si
Molar mass 58.155 g·mol−1
Appearance colorless gas
Boiling point −22.8 °C (−9.0 °F; 250.3 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Vinylsilane refers to an organosilicon compound with chemical formula CH2=CHSiH3. It is a derivative of silane (SiH4). The compound, which is a colorless gas, is mainly of theoretical interest.[1]

  1. ^ Ring, M. A.; O'Neal, H. E.; Rickborn, S. F.; Sawrey, B. A. (1983). "Kinetics of the high-temperature thermal decomposition of silanes and alkylsilanes". Organometallics. 2 (12): 1891–4. doi:10.1021/om50006a038.

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Vinylsilane

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Vinylsilane refers to an organosilicon compound with chemical formula CH2=CHSiH3. It is a derivative of silane (SiH4). The compound, which is a colorless...

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Methylsilane

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Heimann, P. J.; Beyene, K. (1995). "Pyrolytic conversion of methyl- and vinylsilane polymers to Si-C ceramics". Journal of Materials Science. 30 (12): 3130–3136...

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Electrophilic substitution of unsaturated silanes

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unsaturated silanes involves attack of an electrophile on an allyl- or vinylsilane. An allyl or vinyl group is incorporated at the electrophilic center...

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List of gases

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10405-27-3 Prop-1-en-1-one or methylketene CH3CH=CO −23 −80 56 6004-44-0 Vinylsilane CH2=CHSiH3 −22.8 58 7291-09-0 Trifluoroiodomethane CF3I −22.5 −110 196...

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Silane

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compounds Methane Germane Stannane Plumbane Related compounds Phenylsilane Vinylsilane Disilane Trisilane Except where otherwise noted, data are given for materials...

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Sakurai reaction

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Smithers, Roger (2004), "The Electrophilic Substitution of Allylsilanes and Vinylsilanes", Organic Reactions, American Chemical Society, pp. 57–575, doi:10.1002/0471264180...

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Lewis acid catalysis

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Teck Peng; Nakai, Takeshi (1 August 1990). "Carbonyl-ene reaction with vinylsilanes: silicon as a controlling element for regio- and stereochemistry". Journal...

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Cathleen Crudden

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Alper, Howard (1 June 1994). "The regioselective hydroformylation of vinylsilanes. A remarkable difference in the selectivity and reactivity of cobalt...

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Vinyl iodide functional group

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Kishi, Yoshito (1996-11-25). "A mild preparation of vinyliodides from vinylsilanes". Tetrahedron Letters. 37 (48): 8647–8650. doi:10.1016/S0040-4039(96)02000-X...

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Vinyllithium

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groups on metal-based reagents, i.e., vinylations. It is a precursor to vinylsilanes, vinylcuprates, and vinylstannanes. It adds to ketones compounds to give...

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