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Structure of 80102-25-6
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(R)-2-((tert-Butoxycarbonyl)amino)-3-(3-chlorophenyl)propanoic acid is a chiral building block featuring a protected amino group and a para-chlorinated aromatic moiety. This bench-stable derivative integrates seamlessly into peptide synthesis workflows, where the tert-butoxycarbonyl group enables orthogonal protection. The molecule’s electron-deficient phenyl ring enhances reactivity in coupling reactions, supporting efficient access to bioactive scaffolds.
(R)-2-((tert-Butoxycarbonyl)amino)-3-(3-chlorophenyl)propanoic acid serves as a valuable chiral building block in peptide synthesis and medicinal chemistry. The protected α-amino acid functionality enables straightforward deprotection and coupling under standard conditions, while the 3-chlorophenyl group provides a handle for further functionalization. Bench-stable and readily purified by chromatography, it facilitates efficient access to bioactive scaffolds and peptidomimetics.
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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: