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Structure of 149876-86-8
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1,3-Di-(N-Boc-amino)-2-aminopropane features two N-Boc-protected amine groups flanking a central primary amine, enabling sequential deprotection and functionalization. This triamine scaffold supports the synthesis of complex peptide mimetics, dendritic architectures, and multifunctional ligands under standard bench conditions.
1,3-Di-(N-Boc-amino)-2-aminopropane serves as a versatile bifunctional building block for peptide and heterocyclic synthesis. The Boc-protected amines offer orthogonal reactivity and enhanced bench stability, facilitating sequential coupling without side protection. Its triamine architecture enables efficient scaffold diversification in macrocyclic and peptidomimetic libraries, with demonstrated utility in solid-phase and solution-phase workflows.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: