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Structure of 214750-71-7
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This fluorenylmethoxycarbonyl-protected indoline derivative features a stable, bench-handled scaffold ideal for peptide synthesis. The C-terminal carboxylic acid group enables direct coupling, while the octahydroindole ring provides enhanced solubility and reduced aggregation in polar solvents.
(2S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)octahydro-1H-indole-2-carboxylic acid serves as a robust chiral building block for peptide synthesis, enabling efficient N-terminal protection of amino acids. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability under basic conditions and facilitates straightforward removal via mild base treatment. Its octahydroindole scaffold offers defined stereochemistry and functional group compatibility, supporting diverse coupling reactions in solid-phase and solution-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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: