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Structure of 1220220-21-2
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N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]acetamide features a pyridine-linked boronate ester enabling efficient Suzuki-Miyaura coupling. The tetramethyl-dioxaborolane moiety confers excellent stability and compatibility with aqueous conditions, while the acetamide group enhances solubility and facilitates downstream functionalization in medicinal chemistry and materials synthesis.
N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]acetamide serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. The pyridylboronate moiety enables efficient Suzuki-Miyaura coupling under mild conditions, while the acetamide group provides stability and facilitates purification. This compound exhibits excellent bench stability, functional group tolerance, and compatibility with diverse reaction scopes in medicinal chemistry and materials synthesis.
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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: