Weight | 164.204 g/mol |
---|---|
Formula | C10H12O2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
4-Isopropylbenzoic acid (536-66-3)
cumic acid · 4-isopropylbenzoate · p-cumate
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- Bacterial metabolism of side chain fluorinated aromatics: cometabolism of 4-trifluoromethyl(TFM)-benzoate by 4-isopropylbenzoate grown Pseudomonas putida JT strains (Archives of Microbiology, 1988)
- Process of preparing cumic acid (1939)
- Monocyclic terpene alcohols. IV. Birch reduction of p-isopropylbenzoic acid (cumic acid) (Journal of Organic Chemistry, 1967)
- Liquid chromatographic analysis in mouse, dog and human plasma; stability, absorption, metabolism and pharmacokinetics of the anti-HIV agent 2-chloro-5-(2-methyl-5,6-dihydro-1,4-oxathiin-3-yl carboxamido) isopropylbenzoate (NSC 615985, UC84) (Journal of Pharmaceutical and Biomedical Analysis, 1998)
- Studies on the Utilization of Hydrocarbons by Microorganisms: Part XI. Effects of Organic Nutrients, Mineral Salts and Other Substances on the Accumulation of Cumic Acid from p-Cymene (Agricultural and biological chemistry, 1968)
- Process for producing cumic acid (1968)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cumic acid
- 4-isopropylbenzoate
- p-cumate
-
SMILESCC(C)C1=CC=C(C=C1)C(=O)O
-
InChIKeyCKMXAIVXVKGGFM-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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