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Structure of 14676-01-8
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This protected phenylalanine derivative features a tert-butoxycarbonyl group that confers bench stability and facilitates straightforward deprotection. The pendant phenyl ring enhances aromatic character, while the carboxylic acid functionality enables coupling reactions in peptide synthesis workflows under standard conditions.
3-((tert-Butoxycarbonyl)amino)-3-phenylpropanoic acid serves as a valuable building block in peptide synthesis and medicinal chemistry, enabling the introduction of phenyl-substituted amino acid motifs with high functional group tolerance. The Boc-protected amine and carboxylic acid functionalities facilitate sequential coupling reactions and orthogonal deprotection strategies. Its bench-stable nature and straightforward purification support scalable synthesis workflows in API development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: