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Structure of 847818-56-8
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized pyrazole derivatives with high efficiency. The ethyl substituent enhances solubility and stability in polar solvents, while the pyrazole core provides a rigid, electron-rich scaffold ideal for medicinal chemistry applications.
(1-Ethyl-1H-pyrazol-4-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The pyrazole moiety provides enhanced stability and solubility compared to simpler boronic acids, while the ethyl substituent improves crystallinity and simplifies purification. Its compatibility with diverse functional groups makes it ideal for late-stage functionalization in medicinal chemistry and process development workflows.
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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: