CAS 2916-68-9
:2-(Trimethylsilyl)ethanol
- (2-Hydroxyethyl)trimethylsilane
- 2-(Trimethylsilanyl)ethanol
- 2-(Trimethylsilyl)ethan-1-ol
- 2-(Trimethylsilyl)ethyl alcohol
- Ethanol, 2-(trimethylsilyl)-
- NSC 96784
- O-(2-Mesitylenesulfonyl)acethydroxaMic acid ethyl ester
- β-(Trimethylsilyl)ethanol
- 2-(Trimethylsilyl)ethanol
- 2-(Trimethylsilyl) ethanol
- 2-(TRIMETHYLSILYL)ETHANAL
- Silane, (2-hydroxyethyl)trimethyl-
- 2-HYDROXYETHYLTRIMETHYLSILANE
- 2-(TRIMETHYLSILYL)ETHANOL, 98+%
- (2-hydroxyethyl)trimethyl-silan
- TIMTEC-BB SBB009030
- trimethylsilylethanol
- See more synonyms
2-(Trimethylsilyl)ethanol
CAS:Formula:C5H14OSiPurity:>96.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:118.252-(Trimethylsilyl)ethanol, 98+%
CAS:2-(Trimethylsilyl)ethanol is used as a protecting reagent for carboxyl, phosphoryl, hydroxyl and amino group in organic synthesis. It is used as a precursor to prepare trimethyl(2-phenoxyethyl)silanes by reacting with aromatic fluoride. It is also used in the synthesis of teoc-protected amines by u
Formula:C5H14OSiPurity:98+%Color and Shape:Clear colorless, LiquidMolecular weight:118.25Ethanol, 2-(trimethylsilyl)-
CAS:Formula:C5H14OSiPurity:97%Color and Shape:LiquidMolecular weight:118.24962-(Trimethylsilyl)ethan-1-ol
CAS:2-(Trimethylsilyl)ethan-1-olFormula:C5H14OSiPurity:99%Color and Shape: clear. colourless liquidMolecular weight:118.25g/mol2-(Trimethylsilyl)ethanol
CAS:Controlled ProductFormula:C5H14OSiColor and Shape:NeatMolecular weight:118.252-Trimethylsilylethanol
CAS:S19375 - 2-Trimethylsilylethanol
Formula:C5H14OSiPurity:95%Color and Shape:ClearMolecular weight:118.2512-(Trimethylsily)ethanol
CAS:2- (Trimethylsily)ethanol is a hdac inhibitor that is used in the synthesis of other chemical substances. It inhibits HDAC activity by binding to the hydroxyl group on the histone and prevents acetylation of lysine residues, preventing gene transcription. 2-(Trimethylsily)ethanol has been shown to inhibit oxidation reactions in biological systems, such as those caused by trifluoroacetic acid or trichloroacetic acid. In addition, this reagent can be used to prepare functional groups through a synthetic method with an activation energy of 15 kcal/mol and a reaction rate constant of 0.04 M-1 s-1. 2-(Trimethylsily)ethanol has also been used for preparative methods with cleavage products including sulfamoyl chloride.
Formula:C5H14OSiPurity:95%NmrColor and Shape:PowderMolecular weight:118.25 g/mol






