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Structure of 2480-96-8
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Methyl (S)-2-amino-5-((tert-butoxycarbonyl)amino)pentanoate hydrochloride serves as a key chiral building block for peptide synthesis, featuring a protected amino group and a methyl ester functionality. The tert-butoxycarbonyl moiety ensures stability during reaction sequences, while the hydrochloride salt enhances solubility and handling under standard bench conditions.
Methyl (S)-2-amino-5-((tert-butoxycarbonyl)amino)pentanoate hydrochloride serves as a versatile chiral building block for peptide synthesis and medicinal chemistry applications. The protected α-amino group and pendant amine enable selective functionalization, while the methyl ester facilitates downstream transformations. Bench-stable and readily purified by recrystallization, it functions effectively in standard coupling protocols and supports the construction of complex heterocyclic scaffolds and peptidomimetics.
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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: