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Structure of 913835-30-0
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized aryl products with high efficiency. The ethoxy substituent enhances solubility in polar aprotic solvents, while the chloro group enables orthogonal reactivity in sequential transformations. Bench-stable and moisture-tolerant, this reagent streamlines synthesis of complex heterocycles and bioactive intermediates.
(2-Chloro-5-ethoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. Its stability under ambient storage and compatibility with diverse functional groups make it ideal for constructing substituted biaryls and heterocyclic scaffolds in medicinal chemistry and materials synthesis. The chloro and ethoxy substituents provide orthogonal reactivity for downstream modifications.
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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-P501
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Lot numbers can be found on the outside label of a product: