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Structure of 144701-20-2
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This fluorenylmethoxycarbonyl-protected hexanoic acid derivative serves as a robust amino acid surrogate in peptide synthesis, featuring a stable C-terminal carboxylate and a photolabile fluorenylmethyl protecting group. The bulky fluorenyl moiety enhances solubility and minimizes racemization during coupling, while the aliphatic chain provides flexibility for backbone integration. Ideal for solid-phase and solution-phase protocols under standard conditions.
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)hexanoic acid serves as a robust N-terminal protecting group for amino acids in peptide synthesis, offering excellent stability under standard coupling conditions and facile removal via mild base treatment. Its fluorenylmethyl (Fmoc) moiety provides high functional group tolerance and enables efficient purification by standard chromatographic methods. The pendant hexanoic acid chain enhances solubility in organic solvents, facilitating use in both solution-phase and solid-phase synthesis 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: