2-(Trimethylsilyl) Ethanol

Catalog Number	ACM2916689-1
CAS Number	2916-68-9
Structure
Synonyms	2-(Trimethylsilyl) Ethal 2-Trimethylsilyl Ethal 2-(Trimethylsilyl)Ethal O-(2-Mesitylenesulfonyl)Acethydroxamic Acid Ethyl Ester 2-(Trimethylsilyl) Ethal O-(2-Mesitylenesulfonyl)Acethydroxamic Acid Ethyl Ester 2-(Trimethylsilyl) Ethal O-(2-Mesitylenesulfonyl)Acethydroxamic Acid Ethyl Ester 2-(Trimethylsilyl) Ethal 2-(Trimethylsilyl)Ethal Trimethylsilylethal 2-(Trimethylsilyl)-Etha 2-(Trimethylsilyl)Ethanal Ethal, 2-(Trimethylsilyl)- 2-Hydroxyethyltrimethylsilane Silane, (2-Hydroxyethyl)Trimethyl-
Molecular Weight	118.25 g/mol
Molecular Formula	C5H14OSi
Boiling Point	71-73 °C(35 mmHg,lit.)
Flash Point	56 °C
Density	0.825 g/mL(25 °C,lit.)
Solubility	Soluble in soluble.
Appearance	Clear colourless liquid
Application	2-(Trimethylsilyl) Ethanol is primarily utilized as a protecting reagent in organic synthesis safeguarding functional groups such as carboxyl phosphoryl hydroxyl and amino groups It serves as an important precursor in the creation of trimethyl(2-phenoxyethyl)silanes through reactions with aromatic fluoride and is integral in synthesizing Teoc-protected amines via alcoholysis with the corresponding isocyanates This versatile compound is instrumental in various protection reactions including those involving phenols acids alcohols hemiacetals and amines and is a significant component in enol ether synthesis and carbohydrate chemistry
Storage	0-6 °C

Custom Reviews

November 08, 2024

"Essential Reagent for Synthesis"

I've used 2-(Trimethylsilyl) Ethanol from Alfa Chemistry in organic synthesis, mainly for protecting functional groups. It's reliable and effective, especially in preparing teoc-protected amines, enhancing our research productivity significantly.

※  Please kindly noted that this product is for research use only.

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