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*For research and further manufacturing use only, not for direct human use.
Structure of 391248-14-9
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This fluorenylmethyl-protected piperidine derivative delivers a robust, bench-stable scaffold for peptide synthesis and bioconjugation. The protected amine enables efficient coupling under standard conditions, while the piperidine ring provides enhanced solubility and structural flexibility in complex molecular architectures.
(9H-Fluoren-9-yl)methyl 4-(aminomethyl)piperidine-1-carboxylate hydrochloride serves as a robust, bench-stable building block for peptide and medicinal chemistry applications. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient N-terminal protection in solid-phase synthesis, while the piperidine-based side chain provides a versatile amine handle for conjugation or derivatization. Its hydrochloride salt form enhances solubility and handling, facilitating purification and integration into complex molecular architectures.
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GHS Pictogram :
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GHS No : GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H410
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Precautionary Statements : P273-P391-P501
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Lot numbers can be found on the outside label of a product: