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Structure of 52431-30-8
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2,5-Dibromo-3,4-dinitrothiophene features a highly electron-deficient thiophene core stabilized by dual bromine and nitro substituents. This configuration enables robust coupling in transition-metal-catalyzed reactions, particularly in cross-coupling protocols requiring high reactivity. The molecule exhibits enhanced stability under standard handling conditions while maintaining strong electrophilic character at the ring positions.
2,5-Dibromo-3,4-dinitrothiophene serves as a versatile building block for heterocyclic synthesis, enabling direct functionalization at the 2- and 5-positions via palladium-catalyzed cross-coupling reactions. The dinitro groups enhance electrophilicity at C-3 and C-4, facilitating nucleophilic substitution under mild conditions. Its bench-stable crystalline form supports straightforward handling and purification, making it well-suited for iterative synthesis of complex thiophene-based 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-H315-H319-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: