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Structure of 1309982-17-9
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2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline features a boronate ester group enabling efficient Suzuki-Miyaura coupling under mild conditions. The pendant chloro substituent offers orthogonal reactivity, facilitating sequential functionalization. This bench-stable reagent integrates seamlessly into complex molecule assembly, particularly in medicinal chemistry and materials science applications.
2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline serves as a versatile boron-based building block in Suzuki-Miyaura coupling reactions. The diborane moiety enables efficient cross-coupling with aryl and heteroaryl halides under mild conditions, while the ortho-chloro substituent provides a handle for subsequent functionalization. Its bench-stable, air-tolerant nature and compatibility with diverse reaction partners make it ideal for constructing complex biaryls and heterocyclic 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: