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Structure of 957346-47-3
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2-Ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine features a boronate ester group that enables efficient Suzuki-Miyaura coupling under mild conditions. The ethoxy substituent enhances solubility in organic solvents, while the tetramethyl-substituted dioxaborolane ring ensures high stability and low hydrolytic reactivity. This compound serves as a robust building block for constructing complex heterocyclic architectures in medicinal chemistry and materials science.
2-Ethoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate ester building block for Suzuki-Miyaura cross-coupling reactions. The pyridyl core enables efficient functionalization in medicinal chemistry and materials synthesis, while the tetramethyl-dioxaborolane moiety offers excellent stability, ease of handling, and compatibility with diverse reaction conditions. This reagent facilitates direct coupling with aryl halides and pseudohalides under mild catalytic conditions, enabling rapid assembly of biaryl and heteroaryl scaffolds with predictable regiochemistry.
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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 : H317-H319
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Precautionary Statements : P261-P264-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: