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Structure of 1187927-48-5
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(S)-1-Boc-amino-butyl-3-amine features a chiral backbone with orthogonal functional groups, enabling selective derivatization in peptide and macrocyclic synthesis. The Boc-protected amine ensures stability during handling, while the primary amine at the terminal position facilitates conjugation under mild conditions. This scaffold supports efficient incorporation into bioactive architectures requiring defined stereochemistry and controlled reactivity.
(S)-1-Boc-amino-butyl-3-amine serves as a chiral building block for the synthesis of bioactive amines and peptide-like scaffolds. Its Boc-protected amine and terminal primary amine enable sequential functionalization in multistep syntheses. The molecule exhibits excellent bench stability, facilitates straightforward purification via chromatography or crystallization, and functions effectively in standard coupling reactions. Widely used in medicinal chemistry workflows, it enables access to structurally diverse compounds with defined stereochemistry.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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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: