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Structure of 1515866-60-0
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This boronate-functionalized pyridooxazine integrates seamlessly into Suzuki-Miyaura coupling reactions, offering enhanced stability and predictable reactivity under standard conditions. The tetramethylborolane moiety enables efficient cross-coupling, while the dihydrooxazine scaffold provides a rigid, electron-rich platform for downstream derivatization in medicinal chemistry and materials synthesis.
7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. Its stable tetramethylboronate group enables efficient C–C bond formation under mild conditions, with excellent functional group tolerance and bench stability. The dihydrooxazine core provides a rigid, polar scaffold suitable for medicinal chemistry applications, facilitating the construction of complex heterocyclic architectures in drug discovery workflows.
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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: