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Structure of 162607-15-0
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions, delivering arylated products with high functional group tolerance. The methylthio substituent enhances stability and solubility under standard conditions, enabling efficient synthesis of complex heteroaromatic frameworks in medicinal chemistry and materials science applications.
(4-Methylthiophen-2-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 exhibits good bench stability and moderate functional group tolerance, facilitating straightforward purification and integration into complex molecular architectures. Its thienyl scaffold provides a robust heterocyclic core relevant to pharmaceutical and agrochemical research.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: