N-(4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononyl)iodoacetamide, an organic compound widely utilized in chemical synthesis, serves as a crucial tool in various research and industrial applications. Known for its unique reactivity and selectivity, this compound plays a key role in peptide chemistry and bioconjugation processes. Its ability to selectively modify thiol groups in peptides and proteins makes it an invaluable reagent in the development of bioconjugates and in the study of protein structures and functions.In chemical synthesis, N-(4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononyl)iodoacetamide is commonly employed for the selective alkylation of sulfhydryl groups in peptides and proteins. This alkylation reaction forms stable carbon-sulfur bonds, allowing for the precise modification of target molecules. Furthermore, the tridecafluorononyl group confers enhanced hydrophobicity and stability to the modified compounds, making them ideal for various applications in chemical biology, proteomics, and drug discovery.Overall, N-(4,4,5,5,6,6,7,7,8,8,9,9,9-Tridecafluorononyl)iodoacetamide proves to be an indispensable reagent in chemical synthesis, enabling researchers to design and create novel bioconjugates, probe protein structures, and advance our understanding of complex biological processes.
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