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Structure of 145038-53-5
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N-9-Fluorenylmethoxycarbonylaspartic acid β-methyl ester features a fluorenylmethoxycarbonyl (Fmoc) group for orthogonal protection in peptide synthesis, paired with a β-methyl ester that enhances metabolic stability. This derivative enables efficient incorporation of aspartic acid analogs into complex sequences under standard coupling conditions, offering improved solubility and reduced side reactions during chain elongation.
N-9-Fluorenylmethoxycarbonylaspartic acid β-methyl ester serves as a robust diacid building block for peptide synthesis, enabling selective protection of both α- and β-carboxyl groups. Its fluorenylmethoxycarbonyl (Fmoc) group ensures orthogonal deprotection under mild basic conditions, while the β-methyl ester enhances metabolic stability and modulates steric profile. The compound exhibits excellent bench stability, simplifies purification, and functions reliably in standard solid-phase and solution-phase workflows.
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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: