rel-Ethyl(1R,2S)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropane-1-carboxylate

98%

Reagent Code: #186019
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CAS Number 2135443-14-8

science Other reagents with same CAS 2135443-14-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.10 g/mol
Formula C₁₂H₂₁BO₄
badge Registry Numbers
MDL Number MFCD32066801
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing cyclopropane-containing structures. The ethyl ester functionality allows for further synthetic manipulation, such as hydrolysis or reduction, to access a range of functionalized cyclopropane derivatives important in bioactive compound development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,030.00
inventory 250mg
10-20 days ฿19,760.00
inventory 500mg
10-20 days ฿30,840.00
inventory 1g
10-20 days ฿40,150.00
rel-Ethyl(1R,2S)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropane-1-carboxylate
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research for constructing cyclopropane-containing structures. The ethyl ester functionality allows for further synthetic manipulation, such as hydrolysis or reduction, to access a range of functionalized cyclopropane derivatives important in bioactive compound development.
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