Weight | 186.403 g/mol |
---|---|
Formula | C8H18OSi2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 4 |
1,3-Divinyltetramethyldisiloxane (68083-19-2, 2627-95-4)
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- Polymerization by Hydrosilation. 2. Preparation and Characterization of High Molecular Weight Poly[(1,1,3,3-tetramethyldisiloxanyl)ethylene] from 1,3-Dihydridotetramethyldisiloxane and 1,3-Divinyltetramethyldisiloxane (Macromolecules, 1994)
- Preparation, Characterization, and X-ray Structure of the 1:1 Complex of o-Acetylstyrene and Carbonylbis(triphenylphosphine)ruthenium. A New Catalyst for the Copolymerization of Acetophenone and 1,3-Divinyltetramethyldisiloxane (Organometallics, 1998)
- End group analysis accounts for the low molecular weight observed in the 1,3-divinyltetramethyldisiloxane-Pt complex catalyzed hydrosilylation copolymerization of , -dienes and 1,3-dihydridotetramethyldisiloxane (Macromolecules, 1999)
- Cyclopolymerization of Metalloid-Containing Alpha, Omega-Dienes. 1.3- Divinyltetramethyldisiloxane, 1,3-Divinyltetramethyl-Disilazanr and 1.3- Divinylpentamethyldisilazane (Macromolecules, 1993)
- Ruthenium catalyzed polymerization of 4acetylstilbenes and 1,3divinyltetramethyldisiloxane (Macromolecular Rapid Communications, 1997)
- Ruthenium-catalysed copolymerization of 4-benzoylpyridine or benzophenone and 1,3-divinyltetramethyldisiloxane Competition between formation of cyclic co-monomers and linear copolymers (Polymer, 1999)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC[Si](C)(C=C)O[Si](C)(C)C=C
-
InChIKeyBITPLIXHRASDQB-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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