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Structure of 1219931-41-5
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This tetrahydropyridine derivative features a boronate ester group for efficient cross-coupling reactions, paired with a trifluoroethyl substituent that enhances metabolic stability and lipophilicity. The molecule integrates readily into complex scaffolds under standard conditions.
1,2,3,6-Tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2,2,2-trifluoroethyl)-pyridine serves as a robust boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylborolane moiety ensures excellent stability and ease of handling, while the trifluoroethyl group enhances solubility and metabolic stability in downstream applications. This compound enables efficient construction of functionalized pyridine scaffolds with broad functional group tolerance, facilitating rapid access to complex heterocyclic architectures relevant to medicinal chemistry and materials science.
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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: