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Structure of 369403-30-5
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This protected amino acid derivative features a tert-butoxycarbonyl group enabling stable incorporation into peptide synthesis. The 3,5-dichlorophenyl moiety imparts enhanced lipophilicity and metabolic stability, facilitating efficient conjugation in bioactive molecule design under standard conditions.
2-((tert-Butoxycarbonyl)amino)-2-(3,5-dichlorophenyl)acetic acid serves as a stable, bench-ready building block for peptide and heterocyclic synthesis. The Boc-protected amine enables straightforward deprotection under mild acidic conditions, while the 3,5-dichlorophenyl group provides orthogonal reactivity and enhanced metabolic stability. Its functional group tolerance facilitates use in standard coupling protocols and multi-step sequences.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: