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Structure of 15231-41-1
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Boc-C2-NH2 delivers a protected primary amine functionality with enhanced stability and ease of handling. This bench-stable reagent integrates readily into peptide coupling sequences, enabling efficient incorporation of aminoethyl units. The tert-butoxycarbonyl group ensures reliable protection under standard conditions, while the ethylene spacer provides optimal flexibility for downstream deprotection and functionalization.
Boc-C2-NH2 serves as a versatile building block for the synthesis of amino acid derivatives and bioactive peptides. The tert-butyl carbamate (Boc) group provides excellent stability under basic conditions and facilitates straightforward deprotection with mild acids. Its terminal primary amine enables efficient coupling reactions, while the ethylene linker offers conformational flexibility, making it well-suited for solid-phase peptide synthesis and the construction of heterocyclic scaffolds in medicinal chemistry applications.
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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 : H227-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: