Thietane
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Names | |||
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IUPAC name
Thietane | |||
Other names
Thiacyclobutane Trimethylene sulfide | |||
Identifiers | |||
102383 | |||
287-27-4 | |||
ChemSpider | 8895 | ||
EC number | 206-015-0 | ||
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Jmol-3D images | Image | ||
PubChem | 9251 | ||
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UN number | 1993 | ||
Properties | |||
Molecular formula |
C3H6S | ||
Molar mass | 74.14 g·mol−1 | ||
Appearance | Colourless liquid | ||
Odor | Sulfurous | ||
Density | 1.028 g cm−3 | ||
Boiling point | 94 °C (201 °F; 367 K) | ||
Hazards | |||
GHS pictograms | |||
GHS signal word | DANGER | ||
H225, H302 | |||
P210 | |||
EU classification | F Xn | ||
R-phrases | R11, R22 | ||
S-phrases | S16 | ||
NFPA 704 | |||
Flash point | -11(9) °C | ||
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |||
verify (what is: / ?) | |||
Infobox references | |||
Thietane is a heterocyclic compound containing a saturated four-membered ring with three carbon atoms and one sulfur atom.[1][2]
References
- ↑ Leśniak, S; Lewkowski, J; Kudelska, W; Zając, A (2008). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry III 2.07: 389–428. doi:10.1016/B978-008044992-0.00207-8.
- ↑ Block, E; DeWang, M (1996). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry II 1.24: 773–802. doi:10.1016/B978-008096518-5.00024-1.