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Structure of 120289-22-7
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This acetic acid derivative features a tert-butoxy carbonyl group flanked by a reactive ester moiety, enabling selective conjugation in peptide synthesis. The pendant tert-butyl ester provides enhanced stability and ease of purification, while the α-ester functionality facilitates orthogonal deprotection under mild acidic conditions. Ideal for site-specific derivatization in bioconjugation workflows.
2-[2-(tert-Butoxy)-2-oxoethoxy]acetic acid serves as a versatile building block for the synthesis of β-keto ester derivatives and protected acetyl intermediates. Its tert-butoxycarbonyl (Boc) group provides orthogonal protection under mild acidic conditions, enabling selective deprotection in complex molecule assembly. The molecule facilitates efficient coupling reactions and functions effectively in peptide and heterocyclic scaffold construction due to its bench-stable nature and compatibility with standard synthetic protocols.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: