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Structure of 171663-13-1
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tert-Butyl (3-bromobenzyl)carbamate delivers a protected amine handle via a stable carbamate linkage, enabling straightforward deprotection under mild acidic conditions. The meta-bromophenyl moiety supports direct functionalization in cross-coupling reactions and provides a robust anchor for synthetic diversification in medicinal chemistry and materials development.
tert-Butyl (3-bromobenzyl)carbamate serves as a versatile protecting group for primary amines, enabling selective functionalization in complex molecule synthesis. The ortho-bromo substituent provides a handle for subsequent cross-coupling reactions, while the tert-butyl carbamate moiety offers excellent bench stability and facile removal under mild acidic conditions. Its compatibility with palladium-catalyzed transformations and broad functional group tolerance make it a reliable building block for medicinal chemistry and API intermediate 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-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: