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Structure of 177735-10-3
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized heteroaryl products with high efficiency. The methylthiophene scaffold provides enhanced stability and solubility in organic media, facilitating straightforward handling and purification.
(2-Methylthiophen-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. The boronic acid moiety offers excellent bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into complex molecular architectures. Its thiophene core provides a rigid, electron-rich scaffold valuable for constructing bioactive heterocycles and advanced materials.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: