ethyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclopentane-1-carboxylate

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Reagent Code: #183992
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CAS Number 2365173-44-8

science Other reagents with same CAS 2365173-44-8

blur_circular Chemical Specifications

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Weight 280.17 g/mol
Formula C₁₅H₂₅BO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily 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 cyclopentane frameworks. The ethyl ester functionality allows further derivatization, such as hydrolysis or reduction, to access carboxylic acids or alcohols in target molecules. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,320.00
inventory 500mg
10-20 days ฿12,960.00
inventory 1g
10-20 days ฿20,250.00
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ethyl 3-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclopentane-1-carboxylate
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Used primarily 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 cyclopentane frameworks. The ethyl ester functionality allows further derivatization, such as hydrolysis or reduction, to access carboxylic acids or alcohols in targe

Used primarily 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 cyclopentane frameworks. The ethyl ester functionality allows further derivatization, such as hydrolysis or reduction, to access carboxylic acids or alcohols in target molecules. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug discovery.

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