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Structure of 956364-44-6
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This pyrazole-acetic acid derivative features a methyl-substituted pyrazole ring linked to a carboxylic acid via a methylene bridge. The electron-rich heterocycle enhances solubility and reactivity in synthetic transformations. It serves as a key scaffold for bioactive molecule development, particularly in kinase inhibitor design and medicinal chemistry campaigns requiring polar, hydrogen-bonding motifs.
2-(4-Methyl-1H-pyrazol-1-yl)acetic acid serves as a versatile building block for medicinal chemistry campaigns, enabling the construction of pyrazole-containing scaffolds via standard amide coupling and conjugation reactions. Its bench-stable nature, combined with good solubility and compatibility with common protecting group strategies, facilitates efficient synthesis of target molecules in drug discovery 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 : 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: