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6213-94-1

Vinyloxytrimethylsilane

Catalog#: AR003W0L  |   CAS#: 6213-94-1  |   MDL#: MFCD00054764  |   MF: C5H12OSi  |   MW: 116.23367999999999

Packsize Purity Price Availability Quantity
250mg 95% $7.00 Global Stock Buy Now Add To Cart
1g 95% $9.00 Global Stock Buy Now Add To Cart
5g 95% $32.00 Global Stock Buy Now Add To Cart
10g 95% $42.00 Global Stock Buy Now Add To Cart
25g 95% $81.00 Global Stock Buy Now Add To Cart
100g 95% $229.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003W0L
Chemical Name Vinyloxytrimethylsilane
CAS Number 6213-94-1
Molecular Formula C5H12OSi
Molecular Weight 116.23367999999999
MDL Number MFCD00054764
SMILES C=CO[Si](C)(C)C

Vinyloxytrimethylsilane, also known as siloxyvinyltrimethylsilane, is a versatile organosilicon compound frequently employed in chemical synthesis as a valuable building block. In organic chemistry, this compound serves as a precursor in various reactions, offering unique reactivity and functionality that enable the production of a wide range of valuable products.One prominent application of vinyloxytrimethylsilane is its participation in the synthesis of vinyl ethers through a process known as the vinyloxytrimethylsilane-promoted Mukaiyama hydration reaction. This reaction involves the addition of water across the double bond of the vinyloxytrimethylsilane, leading to the formation of vinyl ethers. Vinyl ethers are important intermediates in organic synthesis as they can undergo further transformations to yield diverse functionalized compounds.Additionally, vinyloxytrimethylsilane can be utilized in the preparation of α,β-unsaturated carbonyl compounds via the vinyloxytrimethylsilane-promoted Horner-Wadsworth-Emmons reaction. This reaction involves the reaction of vinyloxytrimethylsilane with aldehydes or ketones to afford the corresponding α,β-unsaturated esters or phosphonates. These α,β-unsaturated carbonyl compounds are useful precursors in the synthesis of various pharmaceuticals, agrochemicals, and natural products.Furthermore, vinyloxytrimethylsilane can also participate in cross-coupling reactions, leading to the formation of carbon-carbon or carbon-heteroatom bonds. The presence of the silyloxy group in vinyloxytrimethylsilane imparts stability and enhances the reactivity of the compound in various transformations.In conclusion, vinyloxytrimethylsilane's unique reactivity and versatility make it a valuable tool in chemical synthesis, enabling the construction of complex molecular architectures and facilitating the creation of novel compounds with diverse applications in the fields of materials science, pharmaceuticals, and agrochemicals.
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