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Structure of 28547-29-7
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2-Bromo-4-iodobenzoic acid features a benzoic acid core substituted with bromo and iodo groups at the ortho and para positions, respectively. This dual-halogenated scaffold enables efficient cross-coupling transformations in synthetic organic chemistry. The carboxylic acid functionality provides a handle for derivatization, while the halogens offer complementary reactivity in palladium-catalyzed reactions. Bench-stable under standard conditions, this compound serves as a key intermediate in pharmaceutical and materials synthesis.
2-Bromo-4-iodobenzoic acid serves as a versatile dihalogenated benzoic acid scaffold for palladium-catalyzed cross-coupling reactions. Its orthogonal halogen reactivity enables sequential functionalization, with bromine typically undergoing Suzuki or Stille coupling while iodine participates in Buchwald-Hartwig amination or further Sonogashira transformations. The carboxylic acid group facilitates direct derivatization or conjugation, enhancing utility in the synthesis of bioactive heterocycles and pharmaceutical intermediates. Bench-stable and amenable to standard purification methods, it functions reliably in multi-step synthetic sequences.
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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: