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Structure of 33125-05-2
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This bench-stable, moisture-tolerant chiral building block features a protected α-amino acid scaffold with a stereodefined (αR) configuration. The tert-butoxycarbonyl (Boc) group enables straightforward deprotection under mild acidic conditions, while the para-substituted aryl moiety supports efficient coupling reactions in peptide synthesis and medicinal chemistry applications.
(αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]benzeneacetic acid serves as a chiral building block for synthesizing β-amino acid derivatives and peptidomimetics. Its (αR) configuration enables stereocontrolled coupling reactions, while the tert-butoxycarbonyl (Boc) group provides robust protection of the amine under acidic conditions. The compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard peptide coupling protocols.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: