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Structure of 948551-28-8
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This fluorenylmethoxycarbonyl-protected pyrrolidine derivative features a pendant hydroxyl group enabling selective derivatization. The 9-fluorenylmethyl (Fmoc) moiety provides robust protection with facile removal under mild basic conditions, while the hydroxypyrrolidine scaffold offers a versatile chiral building block for peptide and small-molecule synthesis.
(9H-Fluoren-9-yl)methyl 3-hydroxypyrrolidine-1-carboxylate serves as a versatile protected amino acid building block, enabling efficient access to pyrrolidine-containing scaffolds in medicinal chemistry. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability and orthogonal deprotection under mild basic conditions, while the C3 hydroxyl functionality offers a handle for selective derivatization or incorporation into complex molecular architectures. Its compatibility with standard peptide coupling protocols and ease of purification make it a practical choice for solid-phase synthesis and fragment-based drug discovery 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: