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Structure of 19492-95-6
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3-Bromo-5-nitrobenzo[b]thiophene features a fused thiophene core with complementary electron-withdrawing nitro and bromo substituents at meta positions, enabling direct functionalization in cross-coupling reactions. This configuration enhances reactivity while maintaining stability under standard conditions.
3-Bromo-5-nitrobenzo[b]thiophene serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo substituent. The nitro group provides a strong electron-withdrawing effect, enhancing electrophilicity and facilitating subsequent transformations such as reduction to an amine or participation in nucleophilic aromatic substitution. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for constructing complex heterocyclic scaffolds 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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: