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Structure of 1201186-86-8
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This bicyclic amino acid derivative features a tert-butoxycarbonyl-protected amine and a carboxylic acid group, enabling direct incorporation into peptide synthesis. The rigid cage-like structure imparts conformational constraint, enhancing secondary structure stability in bioactive sequences.
4-[(tert-Butoxycarbonyl)amino]bicyclo[2.2.1]heptane-1-carboxylic acid serves as a versatile, bench-stable building block for the synthesis of constrained amino acid derivatives and heterocyclic scaffolds. Its bicyclic core imparts conformational rigidity, while the Boc-protected amine and carboxylic acid enable orthogonal functionalization in peptide and medicinal chemistry workflows. Facilitates efficient coupling reactions and supports diverse downstream transformations under standard conditions.
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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: