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Structure of 93323-67-2
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This pyrazole-based carboxylic acid integrates a sterically hindered diphenylpyrazole moiety with a reactive acetic acid handle, enabling direct conjugation in bioconjugation workflows. The electron-deficient pyrazole ring enhances stability under physiological conditions, while the pendant phenyl groups improve solubility in organic solvents.
2-(3,5-Diphenyl-1H-pyrazol-1-yl)acetic acid serves as a versatile building block for pyrazole-based medicinal chemistry campaigns. Its carboxylic acid functionality enables direct amidation, esterification, or coupling reactions, while the 3,5-diphenylpyrazole core provides structural rigidity and enhanced lipophilicity. The compound exhibits good bench stability and facilitates efficient purification via standard recrystallization or chromatography, supporting scalable synthesis of functionalized heterocyclic scaffolds.
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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 : H315-H319-H335
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Precautionary Statements : P261-P280-P304+P340-P405-P501
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Lot numbers can be found on the outside label of a product: