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Structure of 69190-62-1
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2-Butyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane offers enhanced stability and solubility in organic media compared to standard boronate reagents. The sterically shielded tetramethyl substitution minimizes protodeboronation, while the butyl group improves compatibility with diverse reaction conditions. This bench-stable boronate integrates efficiently into Suzuki-Miyaura coupling workflows, enabling reliable C–C bond formation under mild catalytic activation.
2-Butyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura coupling reactions. Its sterically hindered dioxaborolane core enhances hydrolytic stability and functional group tolerance, facilitating reliable cross-coupling with aryl, heteroaryl, and vinyl halides. The compound functions as a versatile building block in medicinal chemistry and materials synthesis, offering predictable reactivity and straightforward 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: