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Structure of 219819-74-6
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This chiral building block features a protected amino group and a cyclopentyl-substituted aliphatic chain, enabling direct incorporation into peptide architectures. The tert-butoxycarbonyl (Boc) moiety provides stable protection under standard conditions, while the (2R) stereochemistry ensures high fidelity in asymmetric synthesis.
(2R)-2-{[(tert-Butoxy)carbonyl]amino}-3-cyclopentylpropanoic acid serves as a valuable chiral building block for peptide and peptidomimetic synthesis, offering a stable, bench-ready Boc-protected amino acid with defined stereochemistry. Its cyclopentyl side chain provides enhanced hydrophobicity and conformational rigidity, facilitating structure–activity studies in medicinal chemistry. The Boc group enables straightforward deprotection under mild acidic conditions, while the carboxylic acid functionality supports standard 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: