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Structure of 1521114-14-6
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This azetidine-containing carboxylic acid features a tert-butoxycarbonyl-protected amine, enabling stable incorporation into peptide chains. The propanoic acid side chain provides a flexible spacer for conjugation, while the strained azetidine ring imparts unique conformational rigidity. Ideal for medicinal chemistry applications requiring bioactive scaffold integration.
3-(1-(tert-Butoxycarbonyl)azetidin-3-yl)propanoic acid serves as a versatile building block for the synthesis of azetidine-containing bioactive molecules. The tert-butyl ester group provides excellent stability and compatibility with standard peptide coupling conditions, enabling straightforward deprotection under mild acidic conditions. Its propanoic acid side chain facilitates conjugation via amide bond formation, supporting applications in medicinal chemistry and fragment-based drug discovery.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: