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Structure of 1932784-54-7
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This fluorenylmethoxycarbonyl-protected pyrrolidine derivative features a chiral (2S,5S) scaffold with a methyl substituent at the 5-position, enabling stereoselective synthesis in peptide and medicinal chemistry. The Cbz group ensures stable protection during coupling reactions, while the rigid pyrrolidine core facilitates conformational control in complex molecule assembly.
(2S,5S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-5-methylpyrrolidine-2-carboxylic acid serves as a robust chiral building block for peptide synthesis, enabling efficient incorporation of sterically constrained proline analogs. The Fmoc group provides excellent stability and orthogonal deprotection, while the 5-methyl substituent enhances conformational rigidity. This scaffold facilitates the construction of bioactive peptidomimetics and cyclic peptides with predictable secondary structure control, offering reliable handling, high purity, and compatibility with standard solid-phase workflows.
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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: