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Structure of 302333-80-8
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(4-Cyclopropylphenyl)boronic acid features a cyclopropyl group that enhances metabolic stability and lipophilicity, improving cellular permeability. The boronic acid moiety enables reliable Suzuki-Miyaura cross-coupling under standard conditions, delivering arylated products with high functional group tolerance. This bench-stable reagent integrates seamlessly into complex molecule synthesis workflows.
(4-Cyclopropylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. Its cyclopropyl substituent imparts enhanced metabolic stability and favorable lipophilicity profiles, making it particularly valuable for medicinal chemistry applications. The boronic acid moiety exhibits excellent bench stability, tolerance to diverse functional groups, and straightforward purification via crystallization or silica gel chromatography.
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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: