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Structure of 86060-84-6
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a benzyloxy-substituted side chain and a reactive β-ketoacid functionality, enabling direct incorporation into peptide synthesis workflows. The orthogonal protection strategy facilitates selective deprotection and efficient coupling under standard conditions.
(2S)-4-(Benzyloxy)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid serves as a versatile chiral building block for the synthesis of β-amino acid derivatives and peptidomimetics. The fluorenylmethyloxycarbonyl (Fmoc) group enables efficient N-terminal protection in solid-phase peptide synthesis, while the benzyloxy and ketone functionalities offer orthogonal handles for downstream functionalization. Bench-stable and amenable to standard purification methods, it facilitates reliable access to complex scaffolds in medicinal chemistry 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
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Precautionary Statements : P264-P280-P302+P352-P332+P313-P362+P364
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Lot numbers can be found on the outside label of a product: