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Structure of 191529-09-6
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2,4,6-Tribromobenzene-1,3,5-tricarbaldehyde features three bromine substituents at the 2, 4, and 6 positions of a benzene ring, each flanking a formyl group. This symmetrical arrangement delivers a highly electrophilic core ideal for conjugation reactions, particularly in the synthesis of complex molecular architectures. The compound exhibits enhanced stability under standard conditions and facilitates efficient coupling with nucleophiles in multistep transformations.
2,4,6-Tribromobenzene-1,3,5-tricarbaldehyde serves as a versatile tri-functional building block for the synthesis of complex heterocyclic architectures and multi-branched molecular scaffolds. Its three electrophilic aldehyde groups enable efficient coupling reactions under mild conditions, offering high regioselectivity and excellent functional group tolerance. The molecule exhibits robust bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic strategies in medicinal chemistry and materials science applications.
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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: