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Structure of 1310405-06-1
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This boronate-functionalized pyridine integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions. The trifluoromethyl group enhances electron deficiency and metabolic stability, while the tetramethylcyclopentadienone boronate moiety ensures high reactivity and bench-stable handling.
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(trifluoromethyl)pyridine serves as a versatile boronate building block in Suzuki-Miyaura cross-coupling reactions. The tetramethylborolane moiety provides excellent stability and compatibility with diverse reaction conditions, while the trifluoromethylpyridine core enables efficient coupling to aryl and heteroaryl partners. Its bench-stable nature and high functional group tolerance make it ideal for constructing complex pharmaceutical scaffolds and advanced materials.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: