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Structure of 20503-40-6
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6-Aminobenzo[b]thiophene 1,1-dioxide features a fused heterocyclic core with a sulfone group enhancing polarity and metabolic stability. The para-amino substituent provides a reactive handle for conjugation, enabling integration into bioactive scaffolds. This bench-stable compound serves as a key intermediate in the synthesis of kinase inhibitors and fluorescent probes.
6-Aminobenzo[b]thiophene 1,1-dioxide serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of bioactive scaffolds through palladium-catalyzed cross-coupling and electrophilic substitution reactions. The sulfonamide group enhances solubility and metabolic stability, while the amino functionality allows for direct derivatization. Its bench-stable crystalline form facilitates handling and purification in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: