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Structure of 143415-31-0
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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 (S)-configuration ensures stereochemical fidelity in synthetic sequences.
(S)-2-((tert-Butoxycarbonyl)amino)-3-cyclopentylpropanoic acid serves as a valuable chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The Boc-protected amine enables straightforward coupling reactions, while the cyclopentyl group imparts conformational rigidity beneficial in medicinal chemistry optimization. Bench-stable and compatible with standard peptide synthesis protocols, it facilitates efficient purification and functional group manipulation in multi-step sequences.
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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: