Benzyl sulfoxides
Benzyl sulfoxides are a class of organic compounds characterized by the presence of a sulfoxide group (-S=O) attached to a benzene ring. These compounds are widely used in various applications due to their unique chemical properties and structural flexibility. They can be synthesized through different methods, including direct oxidation or reaction of benzenethiol with halides. Benzyl sulfoxides find extensive use as intermediates in the pharmaceutical industry, where they serve as precursors for synthesizing medicinal compounds. Additionally, these compounds are utilized in the production of fragrances and flavorings due to their pleasant aroma profiles. They also play a role in organic synthesis as reagents or protecting groups, facilitating controlled chemical transformations. Research into benzyl sulfoxides continues, exploring their potential applications in catalysis, polymer chemistry, and materials science.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Benzene,1-chloro-4-[(phenylsulfinyl)methyl]- | 17530-80-2 | C13H11ClOS |
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Prosulfocarb Sulfoxide | 51954-81-5 | C14H21NO2S |
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Benzene, [(R)-(phenylmethyl)sulfinyl]- | 20246-02-0 | C13H12OS |
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2,3-dichloro-3-[(4-chlorobenzyl)sulfinyl]-N-(6-methoxy-3-pyridinyl)acrylamide | 337922-27-7 | C16H13Cl3N2O3S |
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2,3-dichloro-N-(6-methoxy-3-pyridinyl)-3-[(4-methylbenzyl)sulfinyl]acrylamide | 1164542-94-2 | C17H16Cl2N2O3S |
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2,3-DICHLORO-3-[(2-CHLOROBENZYL)SULFINYL]-N-(6-METHOXY-3-PYRIDINYL)ACRYLAMIDE | 337922-38-0 | C16H13Cl3N2O3S |
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3-chloro-5-(3-chlorobenzylsulfinyl)-1,2,4-thiadiazole | 486997-74-4 | C9H6Cl2N2OS2 |
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3-[(4-CHLOROBENZYL)SULFINYL]-4-ETHYL-5-([3-(TRIFLUOROMETHYL)PHENOXY]METHYL)-4H-1,2,4-TRIAZOLE | 956607-36-6 | C19H17ClF3N3O2S |
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Benzene, [(S)-(phenylmethyl)sulfinyl]- | 7417-81-4 | C13H12OS |
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Chlorbensid sulfoxide | 7047-28-1 | C13H10Cl2OS |
Related Literature
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
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Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782
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