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Structure of 430460-38-1
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This fluorenylmethoxycarbonyl-protected cyclohexyl amino acid derivative features a rigid, sterically defined scaffold ideal for peptide synthesis. The (1S,2R) stereochemistry ensures precise spatial orientation, while the Fmoc group enables orthogonal deprotection under mild basic conditions. This combination supports efficient coupling and high fidelity in solid-phase and solution-phase sequences.
(1S,2R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexane-1-carboxylic acid serves as a chiral building block for asymmetric synthesis, leveraging the stability and orthogonal deprotection of the Fmoc group. Its cyclohexyl scaffold provides conformational rigidity ideal for peptide backbone modification and medicinal chemistry campaigns. The compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in standard coupling protocols for macrocycle and peptidomimetic construction.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: