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Structure of 865370-16-7
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N-Bocamino-cyano-acetic acid ethyl ester features a protected amine and dual reactive handles—cyano and ester—enabling direct incorporation into peptide backbones or conjugation workflows. The Boc group ensures stability during synthetic manipulations, while the ethyl ester facilitates selective hydrolysis or coupling under mild conditions. This derivative serves as a key building block for non-natural amino acids and bioconjugates in medicinal chemistry.
N-Bocamino-cyano-acetic acid ethyl ester serves as a versatile building block for the synthesis of cyano-containing heterocycles and amino acid derivatives. Its stability under standard reaction conditions, combined with orthogonal functional group compatibility, enables efficient incorporation into peptide-like scaffolds and pharmaceutical intermediates via nucleophilic addition, cyclization, or palladium-catalyzed coupling processes.
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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: