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Structure of 223581-83-7
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(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-oxopyrrolidine-2-carboxylic acid is a bench-stable, moisture-tolerant protected amino acid derivative featuring a fluorenylmethyl carbamate (Fmoc) group. This configuration enables direct incorporation into solid-phase peptide synthesis workflows, offering efficient chain elongation with minimal racemization and clean deprotection under mild basic conditions.
(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-oxopyrrolidine-2-carboxylic acid serves as a valuable chiral building block in peptide synthesis, enabling the construction of sterically constrained proline analogs. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability and orthogonal deprotection under mild basic conditions. Its 4-oxo functionality offers a versatile handle for downstream transformations, including reductive amination and heterocycle formation, while maintaining compatibility with standard coupling protocols and facilitating purification via chromatography or crystallization.
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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: