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Structure of 2196198-73-7
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This fluoren-9-ylmethoxycarbonyl-protected amino acid derivative features a prop-2-enoxycarbonyl-substituted phenyl group, enabling efficient coupling in peptide synthesis. The C-terminal ester facilitates rapid activation and incorporation into oligopeptide chains under standard conditions.
(2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(4-prop-2-enoxycarbonylphenyl)propanoic acid serves as a robust chiral building block for peptide synthesis, enabling efficient formation of sterically constrained C-terminal amino acid derivatives. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability and ease of removal under mild basic conditions, while the prop-2-enoxycarbonyl aryl moiety offers compatibility with standard coupling protocols. Its defined stereochemistry and functional group tolerance facilitate reliable incorporation into complex peptide scaffolds.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P305+P351+P338-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: