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| Names | |
|---|---|
| Preferred IUPAC name
(Methanesulfinyl)benzene | |
| Other names
Methylsulfinylbenzene
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| Identifiers | |
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3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.013.438 |
| EC Number |
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PubChem CID
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| Properties | |
| C7H8OS | |
| Molar mass | 140.20 g·mol−1 |
| Appearance | colorless or white solid |
| Density | 1.19±0.1 g/cm3 |
| Melting point | 32 °C (90 °F; 305 K) |
| Boiling point | 263.5 °C (506.3 °F; 536.6 K) |
| Hazards | |
| GHS labelling: | |
 
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| Warning | |
| H315, H318, H335 | |
| P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Methyl phenyl sulfoxide is the organosulfur compound with the formula CH3S(O)C6H5. A low-melting white solid, it is an oxidized derivative of thioanisole.[1] The compound is a prototypical chiral sulfoxide. As such it has been prepared by asymmetric oxidation.[2]
References[edit]
- ^ Johnson, Carl R.; Keiser, Jeffrey E. (1966). "Methyl Phenyl Sulfoxide". Org. Syntheses. 46: 78. doi:10.15227/orgsyn.046.0078.
- ^ Kagan, Henri B.; Chellappan, Sheela K.; Lattanzi, Alessandra (2015). "(R)-(+)-Phenyl methyl sulfoxide". E-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rn00456. ISBN 978-0471936237.