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Structure of 817562-90-6
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(R)-5-(tert-Butoxy)-5-oxo-4-(4,7,10-tris(2-(tert-butoxy)-2-oxoethyl)-1,4,7,10-tetraazacyclododecan-1-yl)pentanoic acid features a rigid macrocyclic scaffold bearing three pendant tert-butyl ester groups, enabling efficient conjugation and solubility enhancement in aqueous systems. This design supports robust chelation and bioconjugation applications under physiological conditions.
(R)-5-(tert-Butoxy)-5-oxo-4-(4,7,10-tris(2-(tert-butoxy)-2-oxoethyl)-1,4,7,10-tetraazacyclododecan-1-yl)pentanoic acid serves as a versatile bifunctional building block for constructing macrocyclic scaffolds. Its tert-butyl ester and amide functionalities enable orthogonal deprotection strategies, while the pendant carboxylic acid facilitates conjugation via standard coupling reactions. The molecule’s high stability under bench conditions and compatibility with diverse reaction environments support efficient synthesis of complex heterocyclic systems and peptide-coupled constructs.
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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: