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Structure of 81237-69-6
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5-Bromo-1,2,3,4-tetrahydroisoquinoline features a bromine substituent at the 5-position of the tetrahydroisoquinoline core, delivering enhanced reactivity in cross-coupling and functionalization processes. This bench-stable heterocycle integrates readily into pharmaceutical intermediates and bioactive molecule scaffolds due to its favorable electronic profile and solubility.
5-Bromo-1,2,3,4-tetrahydroisoquinoline serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, facilitating the construction of biaryl and heteroaryl architectures. The tetrahydroisoquinoline core provides a rigid, pharmacologically relevant scaffold with favorable solubility and bench stability, supporting efficient functionalization and purification in standard reaction 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: