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Structure of 1072951-54-2
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This boronate moiety features a pyridine core with two chlorine substituents at the 2- and 6-positions, delivering enhanced stability and predictable reactivity in cross-coupling transformations. The electron-deficient heterocycle enables efficient palladium-catalyzed coupling under standard conditions, while the bench-stable nature simplifies handling and storage.
(2,6-Dichloropyridin-4-yl)boronic acid serves as a versatile building block in cross-coupling chemistry, enabling efficient Suzuki-Miyaura reactions under standard conditions. Its pyridine scaffold offers enhanced stability and predictable reactivity, while the ortho-dichloro substitution pattern facilitates sequential functionalization. The boronic acid moiety enables reliable coupling with aryl halides and triflates, making it ideal for constructing complex heterocyclic architectures 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-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: