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Structure of 68373-12-6
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This boronate ester features a reactive iodoethyl group paired with a carbamic acid benzyl ester moiety, enabling efficient coupling in C–N bond formation. The pendant benzyl carbamate offers controlled release and enhanced solubility, while the iodide facilitates palladium-catalyzed transformations under standard conditions.
(2-Iodoethyl)carbamic acid benzyl ester serves as a versatile alkylating agent in synthetic organic chemistry, enabling efficient introduction of the (2-iodoethyl)carbamate moiety. Its stability under standard bench conditions and compatibility with nucleophilic substitution reactions facilitate straightforward incorporation into peptide derivatives, heterocyclic scaffolds, and bioconjugation workflows. The benzyl ester group provides convenient orthogonal protection and facilitates purification via chromatography or crystallization.
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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-H332-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: