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Structure of 1187932-25-7
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tert-Butyl (R)-(1-(3-bromophenyl)ethyl)carbamate is a chiral building block featuring a stereogenic center flanked by a brominated phenyl group and a carbamate-protected amine. This configuration enables direct incorporation into asymmetric synthesis, where the para-bromophenyl moiety supports transition metal-catalyzed coupling reactions. The tert-butyl carbamate group provides stability and facilitates selective deprotection under mild acidic conditions.
tert-Butyl (R)-(1-(3-bromophenyl)ethyl)carbamate serves as a chiral building block for asymmetric synthesis, enabling the construction of enantiomerically pure benzylamine derivatives. Its tert-butyl carbamate group offers excellent bench stability and facile removal under mild acidic conditions, while the pendant 3-bromophenyl moiety supports palladium-catalyzed cross-coupling reactions. The stereochemical integrity is maintained through standard handling, making it a practical choice 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: