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Structure of 281655-37-6
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(S)-4-(((9H-Fluoren-9-yl)methoxy)carbonyl)morpholine-3-carboxylic acid serves as a chiral, bench-stable building block for peptide synthesis. The fluorenylmethyl (Fmoc) group enables efficient N-terminal protection, while the morpholine-3-carboxylic moiety provides a rigid, electron-rich scaffold. This combination supports high coupling efficiency and selective deprotection under standard conditions.
(S)-4-(((9H-Fluoren-9-yl)methoxy)carbonyl)morpholine-3-carboxylic acid serves as a robust chiral building block for peptide and heterocyclic synthesis. Its fluorenylmethoxycarbonyl (Fmoc) group enables efficient, orthogonal protection of primary amines in solid-phase peptide synthesis, while the morpholine-3-carboxylic acid scaffold provides a versatile handle for diversification via standard coupling reactions. The compound exhibits excellent bench stability, clean deprotection profiles, and facilitates purification by standard chromatographic methods.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: