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Structure of 201009-98-5
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(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride is a chiral, bench-stable amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound integrates seamlessly into solid-phase peptide synthesis workflows, enabling efficient N-terminal protection and selective coupling reactions under standard conditions.
(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride serves as a protected amino acid building block for peptide synthesis, enabling efficient N-terminal capping and side-chain compatibility. The Fmoc group ensures orthogonal deprotection under mild basic conditions, while the methyl ester facilitates straightforward conversion to carboxylic acids or amides. Bench-stable and readily purified by chromatography, it functions reliably 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: