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Structure of 36639-50-6
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Sodium (4-nitrophenyl)methanesulfonate serves as a stable, bench-ready sulfonate source for nucleophilic substitution reactions. The para-nitro group enhances electrophilicity at the aromatic ring, enabling efficient coupling under mild conditions. This reagent integrates seamlessly into synthetic workflows requiring activated aryl transfer, offering high solubility and predictable reactivity in aqueous or mixed solvent systems.
Sodium (4-nitrophenyl)methanesulfonate serves as a reliable sulfonate ester reagent for nucleophilic substitution reactions, enabling efficient conversion of alcohols to their corresponding sulfonate derivatives under mild conditions. Its bench-stable crystalline form facilitates handling and purification, while the electron-withdrawing 4-nitrophenyl group enhances leaving group ability. This compound functions effectively in standard coupling protocols and is compatible with diverse functional groups, making it a practical choice for synthetic applications requiring stable, reactive intermediates.
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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-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: