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Structure of 90194-99-3
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(S)-tert-Butyl 2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate features a chiral backbone with orthogonal functional groups: a protected amine and a primary hydroxyl. This bifunctional scaffold enables selective derivatization in peptide synthesis and natural product assembly, offering excellent stability under standard bench conditions.
(S)-tert-Butyl 2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate serves as a versatile chiral building block for peptide and heterocyclic synthesis, enabling efficient access to bioactive scaffolds. The protected amine and primary alcohol functionalities offer orthogonal reactivity, facilitating sequential transformations under standard conditions. Its bench-stable tert-butyl ester and carbamate groups simplify purification and enable scalable derivatization in medicinal chemistry campaigns.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: