(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate
≥95%
science Other reagents with same CAS 220587-29-1
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description Product Description
Used as a key intermediate in the synthesis of biologically active molecules, particularly in pharmaceutical development. Its primary application lies in Suzuki-Miyaura cross-coupling reactions, where the boronate ester group enables efficient carbon-carbon bond formation. This makes it valuable for constructing complex organic structures, especially in the production of chiral amino acid derivatives and peptidomimetics. The presence of the Boc-protected amine and ester functionalities allows for selective deprotection and further derivatization, supporting its use in multi-step syntheses of drug candidates. Commonly employed in research and development of protease inhibitors, receptor agonists, and other therapeutic agents requiring high enantiomeric purity.
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