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Structure of 143426-49-7
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4-(1H-Pyrazol-1-yl)benzenemethanol features a pyrazole ring directly linked to a phenylmethanol scaffold, delivering a versatile pharmacophore for medicinal chemistry. The electron-rich pyrazole moiety enhances hydrogen bonding capacity, while the benzylic alcohol offers a handle for derivatization. This compound exhibits excellent bench stability and solubility in common organic solvents, facilitating use in synthetic transformations and screening campaigns.
4-(1H-Pyrazol-1-yl)benzenemethanol serves as a versatile building block for medicinal chemistry and materials science, enabling the construction of bioactive heterocycles and functionalized aryl systems. The pyrazole moiety provides enhanced metabolic stability and hydrogen-bonding capacity, while the benzylic alcohol facilitates downstream transformations such as oxidation, etherification, or esterification. Its bench-stable nature and compatibility with common coupling reactions make it a practical choice for iterative synthesis campaigns in API development and molecular diversification.
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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: