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Structure of 1936532-04-5
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This fluorenylmethoxycarbonyl-protected amino acid derivative features a sterically constrained, electron-deficient cyclobutane core that enhances backbone rigidity. The 3,3-difluorocyclobutanecarboxylic acid moiety imparts increased metabolic stability and modulates conformational preferences in peptide synthesis. Designed for efficient incorporation into complex peptide sequences under standard coupling conditions.
1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3,3-difluorocyclobutanecarboxylic acid serves as a valuable building block in peptide synthesis, enabling the incorporation of sterically constrained, electron-withdrawing 3,3-difluorocyclobutane motifs. The fluorenylmethyl carbamate (Fmoc) group ensures efficient N-terminal protection with orthogonal deprotection, while the difluorocyclobutane core imparts metabolic stability and modulates conformational flexibility. This compound exhibits excellent bench stability, compatibility with standard coupling reagents, and facilitates purification via standard chromatographic methods.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: