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Structure of 142654-29-3
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This sterically hindered diester delivers exceptional stability and ease of handling in synthetic workflows. The bulky tert-butyl groups shield the reactive ester functionalities, minimizing hydrolysis under ambient conditions. Designed for use in controlled release systems and as a protected precursor in peptide coupling strategies.
Hydroxyimidodicarbonic acid bis(1,1-dimethylethyl) ester serves as a stable, bench-friendly reagent for the efficient formation of imidate esters and subsequent heterocycle synthesis. Its robust functional group tolerance facilitates straightforward derivatization in peptide coupling and glycosylation workflows. The tert-butyl groups confer excellent solubility and ease of purification, making it well-suited for scalable synthetic applications in medicinal chemistry and process 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-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: