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Structure of 22132-99-6
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1-Chloro-4-(S-methylsulfonimidoyl)benzene features a chlorine atom and a sulfonimidoyl group positioned para to each other on a benzene ring, enabling selective coupling reactions. The S-methylsulfonimidoyl moiety offers enhanced stability and tunable reactivity in cross-coupling transformations. This compound serves as a valuable building block for synthesizing functionalized aromatic systems in medicinal chemistry and materials science.
1-Chloro-4-(S-methylsulfonimidoyl)benzene serves as a versatile building block for the synthesis of sulfonamide-containing heterocycles and functionalized aryl scaffolds. The chloro group enables palladium-catalyzed cross-coupling reactions, while the S-methylsulfonimidoyl moiety provides a stable, electron-withdrawing handle compatible with diverse reaction conditions. This compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for iterative synthetic sequences 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-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: