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Structure of 359586-64-4
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This fluorenylmethoxycarbonyl-protected cyclopentanecarboxylic acid derivative features a chiral (1S,2S) backbone ideal for asymmetric synthesis. The Cbz group enables selective deprotection under mild hydrogenolysis conditions, while the rigid cyclopentane scaffold imparts conformational stability. This combination supports efficient peptide coupling and solid-phase synthesis workflows.
(1S,2S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclopentanecarboxylic acid serves as a chiral building block for peptide synthesis, enabling the construction of biologically relevant cyclopentane-containing scaffolds. Its fluorenylmethyl carbamate (Fmoc) protecting group ensures orthogonal deprotection under mild basic conditions, while the rigid cyclopentane core provides defined stereochemistry and conformational restraint. The compound exhibits excellent bench stability and facilitates efficient purification via standard chromatographic methods.
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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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: