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Structure of 1363381-73-0
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2-Methyl-2H-indazole-4-sulfonyl chloride features a reactive sulfonyl chloride group appended to a nitrogen-rich indazole scaffold, enabling direct coupling in heterocyclic synthesis. The methyl substitution enhances regioselectivity and stabilizes the core under standard conditions. This reagent facilitates efficient installation of sulfonyl moieties in medicinal chemistry applications.
2-Methyl-2H-indazole-4-sulfonyl chloride serves as a versatile building block for the synthesis of functionalized indazole derivatives, enabling efficient introduction of sulfonyl groups at the 4-position. Its reactivity facilitates nucleophilic substitution with amines and alcohols under mild conditions, offering high yields and excellent functional group tolerance. The molecule's bench-stable nature and compatibility with standard purification protocols make it well-suited for use in medicinal chemistry campaigns 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 : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: