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Structure of 690632-26-9
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Methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophene-2-carboxylate integrates a boronate handle into a benzo[b]thiophene scaffold, enabling efficient Suzuki-Miyaura coupling. This bench-stable reagent features excellent functional group tolerance and moisture resistance, streamlining the synthesis of complex heteroaryl architectures in medicinal chemistry and materials science.
Methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophene-2-carboxylate serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The boryl group enables efficient C–C bond formation under mild conditions, while the methyl ester and benzo[b]thiophene core provide orthogonal functional handles for further derivatization. Its bench-stable nature, high reactivity, and compatibility with diverse substrates make it ideal for constructing complex heterocyclic scaffolds 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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: