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Structure of 1231892-80-0
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This boronate-functional aniline integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, offering enhanced stability and moisture tolerance. The ortho-fluoro substituent enables selective activation, while the tetramethyl-substituted dioxaborolane group ensures efficient coupling under mild conditions.
2-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline serves as a versatile boron-containing building block in Suzuki-Miyaura cross-coupling reactions. The boronate ester group enables efficient C–C bond formation under mild conditions, while the ortho-fluoro substituent provides enhanced stability and orthogonal reactivity. This compound exhibits excellent bench stability, straightforward purification, and broad functional group tolerance, making it ideal for constructing complex aromatic scaffolds in medicinal chemistry and materials science applications.
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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: