2-(4,4-bis(Ethoxymethyl)cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

97%

Reagent Code: #185656
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CAS Number 1628927-33-2

science Other reagents with same CAS 1628927-33-2

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Weight 324.26 g/mol
Formula C₁₈H₃₃BO₄
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Storage Room temperature

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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing substituted aromatic and heteroaromatic systems. The ethoxymethyl-protected cyclohexenyl backbone offers stability and controlled reactivity, allowing selective transformations in multi-step syntheses. Commonly employed in the development of functional materials and bioactive molecules where precise molecular architecture is required.

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inventory 100mg
10-20 days ฿14,400.00

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2-(4,4-bis(Ethoxymethyl)cyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing substituted aromatic and heteroaromatic systems. The ethoxymethyl-protected cyclohexenyl backbone offers stability and controlled reactivity, allowing selective transformations in multi-st

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing substituted aromatic and heteroaromatic systems. The ethoxymethyl-protected cyclohexenyl backbone offers stability and controlled reactivity, allowing selective transformations in multi-step syntheses. Commonly employed in the development of functional materials and bioactive molecules where precise molecular architecture is required.

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