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Structure of 247021-90-5
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N-Fmoc-N-methoxy-3-aminopropionic acid features a protected amine and a methoxy-functionalized side chain, enabling direct incorporation into peptide backbones without additional derivatization. The Fmoc group ensures efficient removal under mild basic conditions, while the methoxy moiety enhances solubility and stability during synthesis. This reagent streamlines access to functionalized amino acid building blocks for medicinal chemistry and peptide library development.
N-Fmoc-N-methoxy-3-aminopropionic acid serves as a versatile building block for peptide synthesis and heterocycle construction, enabling efficient incorporation of functionalized amino acid surrogates. The Fmoc group provides orthogonal protection for primary amines, while the methoxy carbamate facilitates controlled release under mild acidic conditions. This compound exhibits excellent bench stability, simplifies purification by chromatography, and tolerates diverse reaction conditions—making it ideal for iterative synthetic workflows in medicinal chemistry and macrocycle 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: