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Structure of 1062238-49-6
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Methyl (R)-3-((tert-butoxycarbonyl)amino)-4-hydroxybutanoate features a chiral hydroxyl-bearing side chain and a protected amine group, enabling selective transformations in peptide and macrocyclic synthesis. The ester functionality supports efficient derivatization, while the tert-butyl carbamate moiety ensures stability under standard bench conditions.
Methyl (R)-3-((tert-butoxycarbonyl)amino)-4-hydroxybutanoate serves as a versatile chiral building block for the synthesis of bioactive heterocycles and peptidomimetics. The protected amine and hydroxyl functionalities enable orthogonal transformations, while the ester group facilitates downstream derivatization. Its bench-stable nature and compatibility with standard coupling and cyclization protocols make it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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: