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Structure of 203854-51-7
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This fluoren-9-ylmethyl carbamate-protected amino acid derivative features a sterically hindered tert-butyl ether group and a chiral (3R) center, enabling reliable incorporation into peptide sequences. The fluorenylmethoxycarbonyl (Fmoc) moiety provides orthogonal protection, while the pendant tert-butoxy functionality enhances solubility and stability under standard coupling conditions.
(3R)-3-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-[(2-methylpropan-2-yl)oxy]butanoic acid serves as a robust, bench-stable chiral building block for peptide synthesis and medicinal chemistry applications. Its structure combines a C-terminal tert-butyl ester with a fluorenylmethoxycarbonyl (Fmoc) protected amine, enabling orthogonal deprotection during solid-phase peptide synthesis. The molecule exhibits excellent functional group tolerance and facilitates efficient coupling reactions under standard conditions, supporting high-yield assembly of complex peptide sequences and peptidomimetic scaffolds.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: