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Structure of 1391630-31-1
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclobutylacetic acid is a chiral building block featuring a fluorenylmethoxycarbonyl (Fmoc) protected amino group and a sterically constrained cyclobutyl side chain. This configuration enables efficient incorporation into peptide sequences under standard coupling conditions, with the Fmoc moiety offering orthogonal protection and ease of removal during synthesis. The cyclobutyl group imparts conformational rigidity, enhancing structural definition in target peptides.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-cyclobutylacetic acid serves as a valuable chiral building block for peptide synthesis, enabling the incorporation of sterically hindered, conformationally constrained amino acid surrogates. The fluorenylmethoxycarbonyl (Fmoc) group provides excellent stability under basic conditions and facilitates straightforward purification via standard chromatographic methods. Its cyclobutyl side chain imparts defined stereochemistry and rigidity, useful in modulating peptide backbone conformation and enhancing metabolic stability in bioactive sequences.
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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: