Introduction of CAS:13735-81-4 | 1-PHENYL-1-TRIMETHYLSILOXYETHYLENE
Trimethyl((1-phenylvinyl)oxy)silane (TMPVOS) is an organosilicon compound that is widely used in a variety of scientific applications. It is a colorless and odorless liquid, with a boiling point of 109°C and a melting point of -75°C. TMPVOS is a highly reactive compound, and its reactivity is due to the presence of the phenylvinyloxy group. TMPVOS is used as a reagent in the synthesis of a variety of organic compounds, and it is also used as a catalyst in organic synthesis. Additionally, TMPVOS is used as a cross-linking agent in the fabrication of polymers, and it is used in the production of polysiloxanes.
Specification of CAS:13735-81-4 | 1-PHENYL-1-TRIMETHYLSILOXYETHYLENE
|
ITEMS |
SPECIFICATION |
|
Melt point |
122-123 °C |
|
Boiling point |
88-89 °C/11 mmHg (lit.) |
|
Density |
0.938 g/mL at 25 °C (lit.) |
|
Refractive index |
n20/D 1.502(lit.) |
|
Purity |
98% |
|
Storage condition |
2-8°C |
|
Form |
clear liquid |
|
Color |
Colorless to Light orange to Yellow |
Related Articles of CAS:13735-81-4 | 1-PHENYL-1-TRIMETHYLSILOXYETHYLENE
Gas-Phase Polymerization: Trimethyl((1-phenylvinyl)oxy)silane undergoes polymerization when exposed to UV laser photolysis, leading to the deposition of polytrimethylsiloxy-substituted polymers. This process is unique and contributes to the field of polymer chemistry (Pola et al., 1997).
Functionalized Benzosiloles Synthesis: This compound facilitates the cyclization of (o-alkynylphenyl)silane into benzosiloles, which are promising materials for organic electronic devices due to their high electron mobility (Ilies et al., 2008).
Thermal Properties in Organosilicon Precursors: Research into the thermal stability and vapor pressure of organosilicon compounds, including trimethyl((1-phenylvinyl)oxy)silane, is crucial for their application in CVD processes (Ermakova et al., 2016).
Protecting Group for Silicon Synthesis: Trimethyl((1-phenylvinyl)oxy)silane is used in synthesizing triorganyl(2,4,6-trimethoxyphenyl)silanes, which serve as reagents in selective cleavage experiments to produce useful chlorosilanes. This has implications for organometallic chemistry and material synthesis (Popp et al., 2007).
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