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*For research and further manufacturing use only, not for direct human use.
Structure of 130309-37-4
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Fmoc-Oic-OH is a protected amino acid derivative featuring a fluorinated indole side chain, designed for efficient incorporation into peptide sequences. This scaffold enhances backbone stability and provides unique steric and electronic profiles beneficial in bioactive peptide design. The Fmoc group enables straightforward solid-phase synthesis under standard conditions.
Fmoc-Oic-OH serves as a valuable building block in peptide synthesis, enabling the incorporation of ortho-iodophenylalanine residues with high fidelity. The Fmoc group provides excellent protection for the amine, allowing for efficient stepwise elongation under standard coupling conditions. The ortho-iodinated aromatic side chain offers a versatile handle for subsequent palladium-catalyzed transformations, facilitating site-specific modifications in complex peptide architectures. Its bench stability and compatibility with common purification methods make it a practical choice for synthetic applications requiring functionalized amino acid units.
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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: