(4-methoxy-2-methylphenylethynyl)trimethylsilane

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Reagent Code: #203908
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CAS Number 1627686-67-2

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blur_circular Chemical Specifications

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Weight 218.37 g/mol
Formula C₁₃H₁₈OSi
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Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex aromatic and conjugated systems. Its ethynyl functionality enables coupling reactions, such as Sonogashira cross-coupling, to build extended π-conjugated molecules for applications in materials science, including organic semiconductors and fluorescent dyes. The trimethylsilyl group acts as a protecting group for the alkyne, allowing selective deprotection and further functionalization. Its methoxy and methyl substituents influence electronic properties and regioselectivity in ring-based reactions, making it valuable in the development of pharmaceuticals and agrochemicals.

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10-20 days ฿36,000.00

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(4-methoxy-2-methylphenylethynyl)trimethylsilane
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Used as a key intermediate in organic synthesis, particularly in the preparation of complex aromatic and conjugated systems. Its ethynyl functionality enables coupling reactions, such as Sonogashira cross-coupling, to build extended π-conjugated molecules for applications in materials science, including organic semiconductors and fluorescent dyes. The trimethylsilyl group acts as a protecting group for the alkyne, allowing selective deprotection and further functionalization. Its methoxy and methyl subst

Used as a key intermediate in organic synthesis, particularly in the preparation of complex aromatic and conjugated systems. Its ethynyl functionality enables coupling reactions, such as Sonogashira cross-coupling, to build extended π-conjugated molecules for applications in materials science, including organic semiconductors and fluorescent dyes. The trimethylsilyl group acts as a protecting group for the alkyne, allowing selective deprotection and further functionalization. Its methoxy and methyl substituents influence electronic properties and regioselectivity in ring-based reactions, making it valuable in the development of pharmaceuticals and agrochemicals.

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