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*For research and further manufacturing use only, not for direct human use.
Structure of 270063-49-5
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Fmoc-(S)-3-Amino-4-(2,4-dichloro-phenyl)-butyric acid is a specialized amino acid derivative featuring a fluorenylmethoxy carbonyl (Fmoc) protecting group and a sterically hindered aromatic moiety. This configuration enhances solubility in organic solvents and provides stability during solid-phase peptide synthesis. The electron-deficient dichlorophenyl ring supports efficient coupling reactions while minimizing side processes. Ideal for incorporating non-natural residues into bioactive peptides, this building block enables precise structural diversification.
Fmoc-(S)-3-Amino-4-(2,4-dichloro-phenyl)-butyric acid serves as a versatile building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The Fmoc group enables efficient solid-phase peptide synthesis, while the 2,4-dichlorophenyl moiety provides enhanced metabolic stability and favorable pharmacokinetic properties. This compound exhibits excellent bench stability, tolerates common reaction conditions, and facilitates straightforward purification—making it ideal for medicinal chemistry campaigns targeting kinase inhibitors and other therapeutic agents.
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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: