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Structure of 707-60-8
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4-Bromo-N,N-dimethyl-benzenesulfonamide features a brominated aromatic ring paired with a sterically hindered sulfonamide group, enabling robust coupling in cross-coupling reactions. The dimethyl substitution enhances solubility and stability under standard conditions, while the para-bromo handle facilitates efficient functionalization in synthetic workflows.
4-Bromo-N,N-dimethyl-benzenesulfonamide serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its bromo group facilitates Suzuki, Stille, and Negishi couplings, while the sulfonamide moiety provides metabolic stability and hydrogen-bonding capacity. The dimethyl substitution enhances solubility and reduces basicity, improving handling and purification. This compound functions reliably in multi-step synthesis of bioactive scaffolds.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: