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*For research and further manufacturing use only, not for direct human use.
Structure of 1607004-16-9
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-isobutoxypropanoic acid is a chiral building block featuring a fluorenylmethyl (Fmoc) protecting group and a sterically hindered isobutoxy side chain. This configuration enables reliable incorporation into peptide synthesis workflows, offering enhanced solubility and stability under standard coupling conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-isobutoxypropanoic acid serves as a valuable chiral building block in peptide synthesis, enabling efficient incorporation of sterically hindered, hydrophobic side chains. The Fmoc group provides orthogonal protection for amines, while the isobutoxypropanoyl moiety offers enhanced solubility and stability during solid-phase synthesis. This derivative facilitates sequence-specific coupling reactions with high fidelity and ease of purification, making it well-suited for the construction of complex peptide scaffolds and medicinal chemistry campaigns requiring precise stereochemical control.
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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: