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Structure of 200335-41-7
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral (3R) configuration and a reactive ketone moiety, enabling site-specific conjugation in peptide synthesis. The C-terminal carbonyl group facilitates efficient coupling reactions under standard conditions, while the fluorenylmethoxycarbonyl group provides robust protection and orthogonal deprotection compatibility. This structure supports the incorporation of biologically active motifs into complex peptides with high fidelity.
(3R)-4-Amino-3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-4-oxobutanoic acid serves as a key chiral building block for the synthesis of peptidomimetics and β-amino acid derivatives. The Fmoc group provides orthogonal protection for the amine, enabling selective deprotection during solid-phase peptide synthesis. Its α,β-unsaturated carbonyl system facilitates conjugate addition reactions and participates in standard coupling protocols with high functional group tolerance. Bench-stable and readily purified by flash chromatography, it functions effectively in multi-step synthetic sequences requiring precise stereocontrol.
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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: