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Structure of 1937236-09-3
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This boronate ester features a difluorinated aniline core, enabling efficient cross-coupling under standard conditions. The tetramethyl-substituted dioxaborolane moiety ensures excellent stability and reactivity in Suzuki-Miyaura transformations. Ideal for constructing complex fluorinated aromatic architectures with high functional group tolerance.
2,3-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The difluorophenyl moiety enhances metabolic stability and modulates electronic properties, while the pinacol boronate group enables efficient coupling under mild conditions. Bench-stable and compatible with diverse functional groups, it facilitates rapid access to fluorinated biaryl scaffolds common in 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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: