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Structure of 22439-61-8
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2-Bromodibenzo[b,d]thiophene serves as a key heterocyclic scaffold for constructing advanced materials in organic electronics. This brominated dibenzo-thiophene derivative features a planar, electron-rich core that facilitates efficient π-conjugation and enhances charge transport properties. The pendant bromine atom enables direct functionalization via transition-metal-catalyzed coupling reactions, streamlining access to complex architectures. Bench-stable and moisture-tolerant, it integrates seamlessly into synthesis workflows requiring high chemical fidelity and reproducibility.
2-Bromodibenzo[b,d]thiophene serves as a versatile building block in the synthesis of functionalized heterocycles and conjugated materials. The bromine substituent enables palladium-catalyzed cross-coupling reactions, facilitating efficient C–C bond formation under standard conditions. Its planar, electron-rich structure enhances π-conjugation, making it valuable for constructing advanced organic semiconductors and pharmaceutical intermediates. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses requiring robust functional group tolerance.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: