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Structure of 1426246-59-4
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This boronate moiety features a morpholine ring and a chlorinated aromatic core, delivering enhanced solubility and stability under standard conditions. The para-chloro substituent enables selective cross-coupling reactions, while the morpholino group improves polarity and reaction compatibility in Suzuki-Miyaura transformations.
(3-Chloro-4-morpholinophenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The morpholino group enhances solubility and modulates electronic properties, while the chlorophenyl boronic acid moiety offers excellent stability and compatibility with diverse functional groups. Ideal for constructing biaryl scaffolds in medicinal chemistry and materials science, it facilitates rapid access to complex molecular architectures with predictable reactivity and straightforward purification.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: