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Structure of 1662682-33-8
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4-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole features a boronate ester group enabling efficient Suzuki-Miyaura coupling, paired with a methyl-substituted thiazole core. This bench-stable reagent integrates readily into C–C bond formations under mild conditions, offering predictable regiochemistry and compatibility with diverse functional groups in synthetic workflows.
4-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazole serves as a robust boronate building block for Suzuki-Miyaura coupling reactions. The sterically hindered tetramethylboronate group enhances stability and minimizes protodeboronation, enabling reliable cross-coupling with aryl and heteroaryl halides under mild conditions. Its thiazole core provides a valuable scaffold for medicinal chemistry and materials science applications, offering good functional group tolerance and ease of purification.
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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: