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Structure of 1225062-60-1
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1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine features a boronate ester group enabling efficient Suzuki-Miyaura coupling. The dihydropyridine core provides a stable, electron-rich scaffold for transition metal-catalyzed transformations. This bench-stable reagent integrates seamlessly into C–C bond formation workflows.
1-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine serves as a versatile boronate building block in palladium-catalyzed cross-coupling reactions. The dihydro-pyridine core provides a stable, bench-accessible scaffold with excellent functional group tolerance, enabling efficient C–C bond formation under mild conditions. Its tetramethyl-substituted boronate moiety ensures high stability and compatibility with aqueous workups, facilitating purification and integration into complex molecular architectures.
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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: