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*For research and further manufacturing use only, not for direct human use.
Structure of 324017-21-2
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(R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-aminophenyl)propanoic acid features a chiral backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct incorporation into peptide synthesis. The para-aminophenyl side chain provides a reactive handle for conjugation and structural diversity in bioconjugate applications. This bench-stable derivative supports efficient coupling under standard conditions.
(R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-aminophenyl)propanoic acid serves as a versatile chiral building block for the synthesis of bioactive peptides and peptidomimetics. The fluorenylmethoxycarbonyl (Fmoc) group enables efficient, orthogonal protection during solid-phase peptide synthesis, while the para-aminophenyl side chain offers a handle for further functionalization. Bench-stable and readily purified by flash chromatography, it facilitates high-yielding coupling reactions under standard conditions.
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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: