Catalog Number | ACM13735814-1 |
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CAS Number | 13735-81-4 |
Structure | ![]() |
Synonyms | A-(Trimethylsilyloxy)Styrene1-Phenyl-1-(Trimethylsilyloxy)Ethylenealpha-(Trimethylsiloxy)Styrenetrimethyl[(1-Phenylethenyl)Oxy]Silane[(1-Fenilvinil)Oxi]Trimetilsila[1-(Trimethylsiloxy)Vinyl]Benzene1-(Trimethylsiloxy)-1-Phenylethene1-(Trimethylsilyloxy)-1-Phenylethene1-(Trimethylsilyloxy)-1-Phenylethylene1-(Trimethylsilyloxy)Styreneseemoresynyms1-Phenyl-1-(Trimethylsiloxy)Ethene1-Phenyl-1-(Trimethylsiloxy)Ethylene1-Phenyl-1-(Trimethylsilyloxy)Etheneacetophenetrimethylsilylelether |
Molecular Weight | 192.33 g/mol |
Molecular Formula | C11H16OSi |
Application | 1-Phenyl-1-trimethylsilyloxyethylene serves a versatile purpose in various chemical syntheses It is prominently used in the formation of β-amino ketones in water through a Mannich-type reaction and in the production of cis-26-disubstituted dihydropyrans via a three-component one-pot cascade reaction Additionally it functions as both a chemical additive and an intermediate This compound a styrene-type silyl enol ether reacts with formaldehyde and 24-pentanedione to produce dihydropyran Furthermore it is involved in the Mukaiyama aldol reaction with aldehydes in aqueous solutions facilitated by amphiphilic calix[6]arene derivatives acting as surfactants |
Excellent Versatility for Research Synthesis
1-Phenyl-1-Trimethylsilyloxyethylene from Alfa Chemistry is a key reagent in my lab, enabling efficient synthesis of β-amino ketones and dihydropyrans. Its role in Mukaiyama aldol reactions has greatly enhanced our research productivity.
※ Please kindly noted that this product is for research use only.