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Structure of 288617-74-3
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This fluoren-9-ylmethoxycarbonyl-protected amino acid features a chiral center at the alpha position and a terminal olefinic handle at C7, enabling efficient conjugation in peptide synthesis. The bulky fluorenylmethoxycarbonyl group provides robust protection, while the methyloct-7-enoic backbone offers enhanced solubility and compatibility with solid-phase workflows.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyloct-7-enoic acid serves as a valuable chiral building block for peptide synthesis, leveraging the robustness of Fmoc protection. Its pendant alkene enables post-functionalization via standard olefin transformations, while the α-methyl group enhances metabolic stability and conformational rigidity. The molecule exhibits excellent bench stability, ease of purification, and compatibility with standard coupling protocols in solid-phase peptide synthesis.
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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-P362+P364-P501
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Lot numbers can be found on the outside label of a product: