Ethyl 1-(3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Cyclopropane-1-Carboxylate
97%
Reagent
Code: #185592
CAS Number
1521255-61-7
blur_circular Chemical Specifications
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Molecular Information
Weight
316.2 g/mol
Formula
C₁₈H₂₅BO₄
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Storage & Handling
Storage
Room temperature
description Product Description
Used primarily as an 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 substituted aromatic and cyclopropane-containing structures. The ethyl ester functionality allows further transformations, such as hydrolysis to the corresponding carboxylic acid or use in peptide-like coupling reactions. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and materials science.
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Ethyl 1-(3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Cyclopropane-1-Carboxylate
Used primarily as an 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 substituted aromatic and cyclopropane-containing structures. The ethyl ester functionality allows further transformations, such as hydrolysis to the corresponding carboxylic acid or use in peptide-like coupling reactions. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and materials science.
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