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Structure of 162607-23-0
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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 dimethylthiophene scaffold imparts enhanced stability and solubility, enabling reliable performance in complex synthetic sequences.
(2,5-Dimethylthiophen-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its thiophene core offers enhanced stability and favorable solubility, while the boronic acid group facilitates reliable coupling under mild conditions. The 2,5-dimethyl substitution pattern provides steric and electronic modulation, improving functional group tolerance and simplifying purification. This reagent is well-suited for medicinal chemistry campaigns requiring access to substituted thiophene derivatives.
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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 : H319
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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: