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Structure of 82132-68-1
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3-Bromo-5,6,7,8-tetrahydroquinoline features a brominated heterocyclic core with enhanced solubility and reactivity in cross-coupling transformations. The saturated quinoline ring system imparts stability while the pendant bromide enables efficient palladium-catalyzed functionalization. This compound serves as a direct precursor for biologically active scaffolds and advanced synthetic intermediates in medicinal chemistry.
3-Bromo-5,6,7,8-tetrahydroquinoline serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the saturated quinoline core offers enhanced solubility and metabolic stability. This compound facilitates efficient access to complex heterocyclic scaffolds and is valued for its bench stability and compatibility with standard reaction conditions.
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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: