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Structure of 1073354-41-2
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This pyridine-based boronate ester integrates a pyrrolidinyl group for enhanced solubility and reactivity, enabling efficient cross-coupling under mild conditions. The tetramethyl-dioxaborolane moiety provides stability and compatibility with standard Suzuki-Miyaura protocols.
2-(Pyrrolidin-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. Its pyrrolidine moiety enhances solubility and stability, while the pinacol boronate group enables efficient coupling with aryl, heteroaryl, and vinyl halides under standard conditions. The compound exhibits excellent bench stability, facilitates straightforward purification, and functions reliably in the construction of complex heterocyclic scaffolds and biaryl architectures common in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: