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Structure of 35036-93-2
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4-Bromobenzo[c][1,2,5]oxadiazole features a fused oxadiazole ring system with a bromine substituent at the para position, enabling direct functionalization in cross-coupling reactions. This electron-deficient heterocycle serves as a stable, bench-ready scaffold for constructing complex bioactive molecules and advanced materials.
4-Bromobenzo[c][1,2,5]oxadiazole serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized heterocycles via palladium-catalyzed cross-coupling reactions. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the oxadiazole core offers enhanced metabolic stability and favorable electronic properties for pharmaceutical scaffolds. Bench-stable and readily purified by flash chromatography, it functions reliably in multi-step syntheses requiring orthogonal reactivity and structural precision.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: