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Structure of 1418132-45-2
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2-Cyclopropoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine delivers a sterically protected boronate group conjugated to a pyridyl scaffold, enabling efficient cross-coupling under mild conditions. The cyclopropoxy substituent enhances solubility and stability, while the tetramethyl-substituted dioxaborolane resists protodeboronation. This reagent streamlines late-stage functionalization in medicinal chemistry workflows.
2-Cyclopropoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile Suzuki-Miyaura coupling partner, enabling efficient C–C bond formation under mild conditions. The boronate ester group exhibits excellent stability, facilitates easy purification, and tolerates a range of functional groups. Its pyridine scaffold provides a valuable building block for heterocyclic synthesis, particularly 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: