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Structure of 247127-51-1
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)propanoic acid is a chiral, protected amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) group and a sterically hindered cyclohexanedione-derived side chain. This structure enables efficient incorporation into peptide synthesis workflows, offering enhanced stability and compatibility with standard coupling protocols.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)propanoic acid serves as a protected amino acid building block for the synthesis of peptidomimetics and constrained peptide scaffolds. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient orthogonal protection, while the 4,4-dimethyl-2,6-dioxocyclohexylidene moiety provides a rigid, sterically defined side chain that facilitates conformational control in bioactive sequences. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for solid-phase peptide synthesis and medicinal chemistry applications.
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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: