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Structure of 4476-28-2
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p-Cymene-7-carboxylic acid features a hydrophobic terpenoid backbone paired with a polar carboxylic acid group, enabling solubility in both organic and aqueous media. This bifunctional architecture supports integration into bioconjugation workflows, drug delivery systems, and polymer synthesis. The molecule exhibits bench-stable handling characteristics and tolerates standard reaction conditions.
p-Cymene-7-carboxylic acid serves as a versatile benzyl-derived building block for the synthesis of functionalized aromatic compounds. Its carboxylic acid functionality enables direct derivatization via esterification, amide formation, or decarboxylation protocols. The pendant isopropyl group enhances lipophilicity and provides steric bulk, supporting its use in medicinal chemistry scaffolds and catalytic ligand design. Bench-stable and readily purified by recrystallization, it functions effectively in standard organic transformations.
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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: