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Structure of 21320-91-2
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2-Methoxy-4-nitrobenzenesulfonyl chloride features a reactive sulfonyl chloride group flanked by electron-withdrawing nitro and electron-donating methoxy substituents, enabling selective derivatization in synthetic organic chemistry. This balance enhances reactivity while maintaining stability under standard conditions.
2-Methoxy-4-nitrobenzenesulfonyl chloride serves as a robust sulfonylating agent for amine functionalization, enabling efficient synthesis of sulfonamide derivatives under mild conditions. Its electron-withdrawing nitro group enhances reactivity while the methoxy substituent provides steric and electronic modulation, improving selectivity in complex molecule synthesis. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for use in medicinal chemistry workflows and API intermediate development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: