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7694-45-3

1-Cyclohexene-1-carboxylicacid, 4-(1-methylethenyl)-

Catalog#: AR005SGY  |   CAS#: 7694-45-3  |   MDL#:  |   MF: C10H14O2  |   MW: 166.217

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Catalog Number AR005SGY
Chemical Name 1-Cyclohexene-1-carboxylicacid, 4-(1-methylethenyl)-
CAS Number 7694-45-3
Molecular Formula C10H14O2
Molecular Weight 166.217
SMILES CC(=C)C1CCC(=CC1)C(=O)O
NSC Number 641067

Perillic acid, a natural compound derived from the oxidation of limonene, finds versatile applications in chemical synthesis. In organic chemistry, perillic acid serves as a valuable building block for the synthesis of various bioactive molecules and pharmaceutical intermediates. Its unique chemical properties, such as the presence of a reactive carboxylic acid group alongside a strained ring system, make it a robust starting material for diverse synthetic routes.One of the significant applications of perillic acid in chemical synthesis is its role as a precursor in the synthesis of perillyl alcohol. Through hydrogenation or reduction reactions, perillic acid can be converted into perillyl alcohol, a compound known for its potential anticancer properties. Perillyl alcohol has been studied for its ability to induce apoptosis in cancer cells and inhibit tumor growth, making it a promising candidate for cancer therapy.Additionally, perillic acid can undergo various chemical transformations to introduce functional groups or structural modifications, enabling the synthesis of novel compounds with desired properties. Its reactivity towards nucleophiles, electrophiles, and radical species allows for the diversification of chemical structures in medicinal chemistry and drug discovery efforts.Overall, perillic acid's versatility in chemical synthesis makes it a valuable tool for creating complex molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.
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