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Structure of 736989-93-8
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Methyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthoate features a boronate ester group appended to a naphthyl scaffold, enabling efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent integrates seamlessly into complex molecule assembly, offering reliable cross-coupling performance with diverse aryl halides.
Methyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-naphthoate serves as a robust boronate building block for Suzuki-Miyaura cross-coupling reactions. The naphthyl core provides a rigid, planar scaffold with defined electronic properties, while the tetramethylborolane group ensures high stability, low toxicity, and excellent functional group tolerance. This reagent facilitates efficient C–C bond formation under mild conditions, enabling rapid access to substituted naphthyl architectures relevant in pharmaceutical and materials synthesis. Its bench-stable nature simplifies handling and purification in routine synthetic workflows.
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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: