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Structure of 172793-31-6
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di-tert-Butyl D-glutamate hydrochloride delivers a sterically shielded, bench-stable D-amino acid derivative ideal for asymmetric synthesis and peptide backbone modification. The protected α-amino and γ-carboxyl groups enable selective coupling under mild conditions, while the hydrochloride salt enhances solubility in common organic solvents. This derivative simplifies access to D-glutamate-containing architectures in medicinal chemistry and catalyst design.
di-tert-Butyl D-glutamate hydrochloride serves as a stable, bench-ready building block for peptide synthesis and medicinal chemistry applications. The di-tert-butyl protection of the glutamate side chain enables orthogonal deprotection in complex sequences, while the hydrochloride salt enhances solubility and handling. It facilitates efficient coupling reactions and is compatible with standard Fmoc-SPPS protocols, offering reliable performance in the construction of peptidomimetics and bioactive scaffolds.
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Lot numbers can be found on the outside label of a product: