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Structure of 943321-89-9
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tert-Butyl N-(5-bromothiophen-2-yl)carbamate features a brominated thiophene scaffold with a bench-stable tert-butyl carbamate protecting group, enabling direct incorporation into cross-coupling and cyclization sequences. The para-bromo functionality facilitates palladium-catalyzed transformations, while the carbamate moiety offers orthogonal protection for amine-directed synthesis in medicinal chemistry and materials development.
tert-Butyl N-(5-bromothiophen-2-yl)carbamate serves as a stable, bench-friendly building block for the synthesis of brominated thiophene-containing scaffolds. The tert-butyl carbamate group provides excellent stability and orthogonal deprotection under mild acidic conditions, enabling sequential functionalization. It readily participates in palladium-catalyzed cross-coupling reactions, facilitating efficient access to biologically relevant heterocyclic architectures and complex molecular frameworks in medicinal chemistry and materials science applications.
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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-H413
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: