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Structure of 1158-35-6
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(R)-Methyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate hydrochloride serves as a chiral building block for peptide synthesis, featuring a protected α-amino group and a pendant benzyloxycarbonyl moiety. This bench-stable derivative facilitates efficient coupling reactions under standard conditions, enabling streamlined access to complex peptide architectures with high diastereoselectivity.
(R)-Methyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate hydrochloride serves as a key chiral building block for the synthesis of bioactive heterocycles and peptide-derived scaffolds. Its amine and ester functionalities enable straightforward coupling reactions, while the benzyloxycarbonyl (Cbz) group provides robust protection under standard conditions. The hydrochloride salt enhances solubility and stability in aqueous and polar organic media, facilitating purification and handling in multi-step syntheses.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: