// Workers AI · dad joke modeWhat did thiazine say to its friend? "Dye" want to hang out?
(Redirected from Thiazines)
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| Names | |
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| Preferred IUPAC name
4H-1,4-Thiazine | |
| Other names
Parathiazine | |
| Identifiers | |
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| ChemSpider | |
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CompTox Dashboard (EPA) |
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| Properties | |
| C4H5NS | |
| Molar mass | 99.15 g·mol−1 |
| Density | 0.8465 g/cm3 |
| Boiling point | 76.5 °C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Thiazine /ˈθaɪəziːn/ is an organic compound containing a ring of four carbon, one nitrogen and one sulfur atom. There are three isomers of thiazine, 1,2-thiazine, 1,3-thiazine, and 1,4-thiazine, which differ by the arrangement of the nitrogen and sulfur atoms in the ring.
Derivatives of thiazine, often referred to as thiazines, are used for dyes, tranquilizers and insecticides.
Preparation
[edit]1,4-thiazine can be prepared by reduction of the corresponding dicarbonyl using aluminium powder at high temperature.[1]
Tautomers
[edit]There are three tautomeric forms:
See also
[edit]- Methylene blue, contains a related ring with nitrogen and a positively charged sulfur atom
- Phenothiazine, a thiazine fused with two benzene rings
- Thiomorpholine, a saturated analog of thiazine
References
[edit]- ↑ Barkenbus, Charles; Landis, Phillip S. (February 1948). "The Preparation of 1,4-Thiazine". Journal of the American Chemical Society. 70 (2): 684–685. Bibcode:1948JAChS..70..684B. doi:10.1021/ja01182a075. ISSN 0002-7863.