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Structure of 51301-86-1
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This protected amino acid derivative features a tert-butoxycarbonyl group that ensures stability and ease of handling, while the para-chlorophenyl substituent imparts enhanced electron-withdrawing character. It integrates readily into peptide synthesis workflows, enabling efficient construction of complex bioactive sequences under standard conditions.
2-((tert-Butoxycarbonyl)amino)-3-(4-chlorophenyl)propanoic acid serves as a versatile building block in peptide synthesis and medicinal chemistry, enabling the introduction of a phenylalanine-derived side chain with enhanced stability. The tert-butyl carbamate (Boc) group provides reliable protection for primary amines during multi-step sequences, while the para-chlorophenyl moiety offers a robust pharmacophoric element. This compound facilitates efficient coupling reactions and is compatible with standard deprotection protocols, supporting scalable synthesis workflows.
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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: