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Structure of 855198-37-7
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2-Bromo-3-iodobenzoic acid features a benzoic acid core substituted with bromine at the ortho position and iodine at the meta position, enabling direct functionalization in cross-coupling reactions. The dual halogenation pattern supports sequential derivatization, while the carboxylic acid group facilitates conjugation or salt formation. This compound serves as a key building block for bioactive molecule synthesis and materials chemistry applications.
2-Bromo-3-iodobenzoic acid serves as a versatile diaryl building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. The orthogonal halogenation pattern facilitates sequential functionalization, while the carboxylic acid group allows for direct derivatization or incorporation into pharmaceutical intermediates. Bench-stable and readily purified by recrystallization, it supports scalable synthesis in 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: