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Structure of 34702-60-8
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This chiral building block features a protected amino group and a perfluorophenyl moiety, enabling efficient coupling reactions in peptide synthesis. The electron-deficient aryl group enhances reactivity in nucleophilic substitution processes, while the tert-butyl ester provides stable storage and selective deprotection under mild acidic conditions.
(S)-2-((tert-Butoxycarbonyl)amino)-3-(perfluorophenyl)propanoic acid serves as a versatile building block for peptide and peptidomimetic synthesis, combining a stable Boc-protected amine with a highly reactive perfluorophenyl ester. The perfluorophenyl group enables efficient coupling to amines under mild conditions, facilitating rapid amide bond formation with high yield and minimal racemization. Its bench-stable solid form simplifies handling and purification, making it ideal for iterative synthetic workflows in medicinal chemistry and API development.
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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-H312-H315-H319
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: