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Structure of 220497-66-5
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(1S,3R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopentanecarboxylic acid is a chiral building block featuring a sterically defined cyclopentane core and a fluorenylmethyl carbamate (Fmoc) protecting group. This configuration enables selective coupling in peptide synthesis, where the Fmoc moiety ensures orthogonal deprotection under mild basic conditions. The molecule exhibits excellent stability under standard bench protocols and integrates cleanly into solid-phase workflows.
(1S,3R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopentanecarboxylic acid serves as a stereochemically defined building block for peptide synthesis, enabling efficient construction of constrained cyclopentane-containing scaffolds. The Fmoc group provides orthogonal protection for primary amines, offering excellent bench stability and facile removal under mild basic conditions. Its functional group tolerance and compatibility with standard coupling protocols facilitate reliable incorporation into complex peptide sequences and medicinal chemistry libraries.
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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: