Acetophenones
Acetophenones are a class of organic compounds characterized by the presence of a phenyl ring fused to an acetyl group. They exhibit a wide range of physical properties, including volatility and solubility in common organic solvents such as dichloromethane and ethyl acetate. Structurally diverse, these compounds can vary significantly based on substituents attached to the benzene ring.
Acetophenones are widely used in various industries due to their versatile applications. In the pharmaceutical sector, they serve as intermediates for drug synthesis. Additionally, they find use in agrochemicals and fragrances, where their characteristic odor profiles make them valuable additives. Acetophenones also exhibit potential antioxidant properties, making them interesting candidates for further research in healthcare applications.
In the manufacturing process, acetophenones can be prepared through various synthetic routes, including condensation reactions of acetyl chloride or acetic anhydride with phenol derivatives. The purity and quality of these compounds are crucial for their successful application across different fields.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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isocaproylbitalin A | 1416142-99-8 | C19H24O4 |
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(+)-oxymycousnine | 130919-04-9 | C19H20O9 |
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1-(4,7-dihydroxy-2-isopropenyl-6-methoxy-2,3-dihydro-benzofuran-5-yl)-ethanone | 32495-02-6 | C14H16O5 |
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1-[2-(1-isobutyryloxymethyl-vinyl)-2,3-dihydro-benzofuran-5-yl]-ethanone | 29048-51-9 | C17H20O4 |
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5-acetyl-2-[1'-(hydroxymethyl)ethyl]-2,3-dihydrobenzo[b]furan | 1070166-35-6 | C13H16O3 |
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3alpha-angeloyloxy-6-hydroxy tremetone | 83212-54-8 | C18H20O5 |
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4-Acetyl-2,3-dihydro-5-hydroxy-2-isopropenylbenzofuran | 110694-79-6 | C13H14O3 |
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(+)-remirol | 26081-40-3 | C14H16O4 |
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O-Angeloyl-Bitalin A | 65580-28-1 | C18H20O4 |
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N/A | 29048-53-1 | C17H20O5 |
Related Literature
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Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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Qiaoe Wang,Meiling Lian,Xiaowen Zhu,Xu Chen RSC Adv., 2021,11, 192-197
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Guang Xu,Wei Zhang,Ying Zhang,Xiaoxia Zhao,Ping Wen,Di Ma RSC Adv., 2018,8, 19353-19361
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Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
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