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Structure of 140898-76-6
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3-Bromo-2-iodobenzo[b]thiophene is a halogenated heterocyclic scaffold featuring strategically positioned bromo and iodo substituents on a benzo[b]thiophene core. This dual-halogenation enables efficient cross-coupling transformations, particularly in palladium-catalyzed reactions, where the distinct reactivity of bromo and iodo groups allows for sequential functionalization. The molecule exhibits robust stability under standard reaction conditions, facilitating its use in constructing complex polycyclic architectures for materials science and pharmaceutical development.
3-Bromo-2-iodobenzo[b]thiophene serves as a versatile biheteroaryl building block for palladium-catalyzed cross-coupling reactions. The orthogonal halogen reactivity enables sequential functionalization, with bromine typically undergoing Suzuki or Stille coupling while iodine participates in Negishi or Sonogashira transformations. Bench-stable and readily purified by flash chromatography, it facilitates the construction of complex fused heterocyclic scaffolds relevant to pharmaceutical and materials chemistry.
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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-P330-P405-P501
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Lot numbers can be found on the outside label of a product: