CAS 31469-15-5
:1-Methoxy-2-methyl-1-(trimethylsiloxy)propene
Dimethylketene Methyl Trimethylsilyl Acetal
CAS:Formula:C8H18O2SiPurity:>95.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:174.321-Methoxy-2-methyl-1-(trimethylsiloxy)propene, 97%
CAS:1-Methoxy-2-methyl-1-(trimethylsiloxy)propene is used in the synthesis of chiral -lactams by reacting with (S)-alkylidene(1-arylethyl)amines in the presence of titanium tetrachloride. It acts as a catalyst or initiator in the group-transfer polymerization. It is also used as a versatile reagent in c
Formula:C8H18O2SiPurity:97%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:174.321-Methoxy-2-methyl-1-(trimethylsiloxy)propene
CAS:Formula:C8H18O2SiPurity:95%Color and Shape:LiquidMolecular weight:174.3128Dimethylketene methyl trimethylsilyl acetal
CAS:Dimethylketene methyl trimethylsilyl acetalPurity:97%Molecular weight:174.31282g/mol(1-Methoxy-2-methylprop-1-enoxy)trimethylsilane
CAS:Controlled ProductStability Moisture and Acid Sensitive
Applications (1-Methoxy-2-methylprop-1-enoxy)trimethylsilane is useful in the synthesis of organic compounds such as 1,1'-Bis[1-(1-methoxycarbonyl-1-methyl-ethyl)-3-butenyl] Ferrocene Monome, Alkylbismuths and N-Tosyl-α,β-dehydroamino Esters.
References Espinosa, M., et al.: RC Adv., 6, 15655 (2016); Nishimoto, T., et al.: Chem. Eur. J., 19, 14411 (2013); Wang, J., et al.: Faming Zhuanli Shenqing, CN 103665053 A 20140326 (2014)Formula:C8H18O2SiColor and Shape:NeatMolecular weight:174.111-Methoxy-1-(trimethylsiloxy)-2-methyl-1-propene
CAS:S11000 - 1-Methoxy-1-(trimethylsiloxy)-2-methyl-1-propene
Formula:C8H18O2SiPurity:95%Color and Shape:LiquidMolecular weight:174.3151-METHOXY-1-(TRIMETHYLSILOXY)-2-METHYL-1-PROPENE
CAS:Trimethylsilyl Blocking Agent
Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.
1- Methoxy-1-trimethysiloxy-2-methyl-1-propene; Methyl(trimethylsilyl)dimethylketene acetal; 1-Methoxy-2-methyl-1-(trimethylsiloxy)propene
Used for silylation of acids, alcohols, thiols, amides and ketonesNafion SAC-13 has been shown to be a recyclable catalyst for the trimethylsilylation of primary, secondary, and tertiary alcohols in excellent yields and short reaction timesSummary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochureFormula:C8H18O2SiPurity:97%Color and Shape:Straw LiquidMolecular weight:174.31Ref: 3H-SIM6496.0
Discontinued product






