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Structure of 721395-15-9
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This chiral cyclopentane scaffold features a Boc-protected amine and a free amino group, enabling direct coupling or selective deprotection in peptide synthesis. The (1R,2S) stereochemistry ensures high diastereoselectivity in cyclization reactions, while the bench-stable Boc group simplifies handling and purification under standard conditions.
(1R,2S)-2-Amino-1-(Boc-amino)cyclopentane serves as a stereochemically defined building block for the synthesis of cyclopentane-containing bioactive molecules. Its protected diamine motif enables sequential functionalization while maintaining configurational integrity. The Boc group ensures stability during storage and facilitates selective deprotection under mild acidic conditions. This compound functions effectively in peptide coupling, heterocycle formation, and scaffold diversification workflows common in medicinal chemistry and process development.
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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#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: