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Structure of 21483-64-7
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tert-Butyl (2-bromothiophen-3-yl)carbamate is a bench-stable, moisture-tolerant building block featuring a brominated thiophene core and a protected amine. This carbamate moiety enables direct incorporation into Suzuki-Miyaura coupling reactions, while the para-bromine facilitates palladium-catalyzed cross-coupling transformations. The structure supports efficient access to functionalized heteroaryl scaffolds in medicinal chemistry and materials science applications.
tert-Butyl (2-bromothiophen-3-yl)carbamate serves as a stable, bench-friendly building block for the synthesis of brominated thiophene derivatives. Its carbamate group enables orthogonal protection during synthetic sequences, while the bromine substituent facilitates palladium-catalyzed cross-coupling reactions such as Suzuki and Stille couplings. The compound exhibits excellent functional group tolerance and is readily purified by flash chromatography, making it well-suited for medicinal chemistry and process development workflows.
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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: