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Structure of 613660-87-0
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This boronic acid features a para-aminosulfonyl group that enhances solubility and facilitates conjugation in bioconjugate chemistry. The boronate moiety enables efficient Suzuki-Miyaura coupling under standard conditions, while the electron-withdrawing sulfonamide imparts stability and directs regioselective functionalization.
(4-Aminosulfonylphenyl)boronic acid serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling the construction of biaryl scaffolds with high functional group tolerance. The pendant sulfonamide group enhances solubility and provides a handle for further derivatization, while the boronic acid moiety offers reliable stability under standard bench conditions and facilitates straightforward purification. Widely employed in medicinal chemistry and materials science, it functions effectively in the synthesis of bioactive heterocycles and conjugated systems.
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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: