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Structure of 219834-94-3
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized naphthalene scaffolds with high efficiency. The methoxy group enhances solubility and modulates electronic properties, while the boronic acid functionality offers reliable stability and compatibility with diverse reaction partners.
(3-Methoxynaphthalen-1-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. Its naphthalene core imparts enhanced stability and solubility, while the methoxy group provides moderate electron-donating character that improves coupling efficiency. The boronic acid functionality offers excellent bench stability, tolerates a range of functional groups, and facilitates straightforward purification—making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: