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Structure of 136099-65-5
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering robust yields under standard conditions. The methyl-substituted benzothiophene scaffold enhances stability and solubility, enabling efficient access to complex heterocyclic architectures in medicinal chemistry and materials science applications.
(5-Methylbenzo[b]thiophen-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. Its bench-stable boronic acid functionality exhibits excellent functional group tolerance and facilitates straightforward purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: