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Structure of 501015-30-1
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxyphenyl)propanoic acid features a chiral center flanked by a fluorenylmethyl carbamate protecting group and a para-methoxyphenyl moiety, enabling direct incorporation into peptide synthesis workflows. This bench-stable derivative supports efficient N-terminal protection with orthogonal deprotection compatibility.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-methoxyphenyl)propanoic acid serves as a robust chiral building block for peptide synthesis and medicinal chemistry applications. The Fmoc group enables efficient N-terminal protection with orthogonal deprotection under mild basic conditions, while the pendant 4-methoxyphenyl moiety provides structural rigidity and enhanced solubility. Its bench-stable nature and compatibility with standard coupling protocols facilitate reliable use in solid-phase and solution-phase syntheses.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: