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*For research and further manufacturing use only, not for direct human use.
Structure of 143415-62-7
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid features a chiral center at the alpha carbon, delivering enantioselective utility in peptide synthesis. The tert-butoxycarbonyl (Boc) group provides robust protection for the amine, while the para-tert-butylphenyl moiety imparts steric bulk and enhanced solubility. This combination enables efficient incorporation into complex peptide architectures under standard coupling conditions.
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid serves as a valuable chiral building block in peptide and medicinal chemistry, enabling efficient synthesis of bioactive scaffolds. The Boc-protected amine and benzylic prochiral center facilitate selective transformations, while the tert-butyl phenyl group provides steric bulk and enhanced solubility. Its bench-stable, crystalline form simplifies handling and purification, making it well-suited for iterative coupling reactions and solid-phase 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: