(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(2-(dimethylamino)ethoxy)phenyl)propanoic acid

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Reagent Code: #38103
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CAS Number 233689-24-2

science Other reagents with same CAS 233689-24-2

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Weight 352.4253 g/mol
Formula C₁₈H₂₈N₂O₅
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a dimethylaminoethoxy phenyl moiety, makes it valuable for designing peptide-based drugs and receptor ligands. Researchers often employ it in the development of enzyme inhibitors or modulators, especially those interacting with amino acid receptors or transporters. Its application extends to the study of drug delivery systems, where its functional groups can enhance solubility and bioavailability of therapeutic agents. Additionally, it is used in the preparation of prodrugs, enabling controlled release and targeted action of active pharmaceutical ingredients.

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inventory 100mg
10-20 days ฿7,533.00

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(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(2-(dimethylamino)ethoxy)phenyl)propanoic acid
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a dimethylaminoethoxy phenyl moiety, makes it valuable for designing peptide-based drugs and receptor ligands. Researchers often employ it in the development of enzyme inh

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a dimethylaminoethoxy phenyl moiety, makes it valuable for designing peptide-based drugs and receptor ligands. Researchers often employ it in the development of enzyme inhibitors or modulators, especially those interacting with amino acid receptors or transporters. Its application extends to the study of drug delivery systems, where its functional groups can enhance solubility and bioavailability of therapeutic agents. Additionally, it is used in the preparation of prodrugs, enabling controlled release and targeted action of active pharmaceutical ingredients.

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