CAS 31469-15-5
:1-Méthoxy-2-méthyl-1-(triméthylsiloxy)propène
Dimethylketene Methyl Trimethylsilyl Acetal
CAS :Formule :C8H18O2SiDegré de pureté :>95.0%(GC)Couleur et forme :Colorless to Almost colorless clear liquidMasse moléculaire :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
Formule :C8H18O2SiDegré de pureté :97%Couleur et forme :Clear colorless to pale yellow, LiquidMasse moléculaire :174.321-Methoxy-2-methyl-1-(trimethylsiloxy)propene
CAS :Formule :C8H18O2SiDegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :174.3128Dimethylketene methyl trimethylsilyl acetal
CAS :Dimethylketene methyl trimethylsilyl acetalDegré de pureté :97%Masse moléculaire :174.31282g/mol(1-Methoxy-2-methylprop-1-enoxy)trimethylsilane
CAS :Produit contrôléStability 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)Formule :C8H18O2SiCouleur et forme :NeatMasse moléculaire :174.111-Methoxy-1-(trimethylsiloxy)-2-methyl-1-propene
CAS :S11000 - 1-Methoxy-1-(trimethylsiloxy)-2-methyl-1-propene
Formule :C8H18O2SiDegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :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 brochureFormule :C8H18O2SiDegré de pureté :97%Couleur et forme :Straw LiquidMasse moléculaire :174.31






