Atomfair tert-Butyl dimethyl(prop-2-en-1-yl)silyl carbonate C10H20O3Si

Description tert-Butyl dimethyl(prop-2-en-1-yl)silyl carbonate (CAS No. 661464-02-4) is a high-purity organosilicon compound with the molecular formula C10H20O3Si . This specialized reagent is widely used in organic synthesis, particularly in protective group chemistry for alcohols and amines. The compound features a reactive allyl group and a tert-butyl carbonate moiety, making it valuable for controlled deprotection strategies. Supplied as a clear, colorless to pale yellow liquid, it is rigorously tested for quality, including GC analysis to ensure >95% purity. Suitable for use under inert atmospheres, this product is packaged in amber glass bottles to ensure stability and longevity. Ideal for researchers in…

Description

tert-Butyl dimethyl(prop-2-en-1-yl)silyl carbonate (CAS No. 661464-02-4) is a high-purity organosilicon compound with the molecular formula C₁₀H₂₀O₃Si. This specialized reagent is widely used in organic synthesis, particularly in protective group chemistry for alcohols and amines. The compound features a reactive allyl group and a tert-butyl carbonate moiety, making it valuable for controlled deprotection strategies. Supplied as a clear, colorless to pale yellow liquid, it is rigorously tested for quality, including GC analysis to ensure >95% purity. Suitable for use under inert atmospheres, this product is packaged in amber glass bottles to ensure stability and longevity. Ideal for researchers in pharmaceuticals, materials science, and fine chemical synthesis.

CAS No: 661464-02-4
Molecular Formula: C10H20O3Si
Molecular Weight: 216.35
Exact Mass: 216.11817103
Monoisotopic Mass: 216.11817103
IUPAC Name: tert-butyl [dimethyl(prop-2-enyl)silyl] carbonate
SMILES: CC(C)(C)OC(=O)O[Si](C)(C)CC=C
Synonyms: 661464-02-4, tert-Butyl dimethyl(prop-2-en-1-yl)silyl carbonate, DTXSID50792761

Application

This compound serves as a versatile protecting group reagent in multi-step organic syntheses, particularly for sensitive functional groups. It demonstrates excellent stability under basic conditions while allowing selective deprotection under mild acidic conditions. Researchers frequently employ it in nucleoside and carbohydrate chemistry to protect hydroxyl groups during complex transformations. The allyl functionality provides additional opportunities for further modification via olefin metathesis or cross-coupling reactions.

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