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Structure of 1873273-39-2
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering naphthalene-based architectures with high efficiency. The chlorine substituent enables orthogonal functionalization, while the bench-stable nature simplifies handling and storage under standard conditions.
(3-Chloronaphthalen-2-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. The naphthalene scaffold provides structural rigidity and π-conjugation, while the boronic acid functionality offers excellent bench stability, compatibility with diverse functional groups, and straightforward purification via crystallization or chromatography. Its utility spans synthetic organic chemistry, materials science, and pharmaceutical development, particularly in constructing biaryl architectures common in advanced intermediates and active pharmaceutical ingredients.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: