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Thietane

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Thietane
Structural formula of thietane
Names
IUPAC name
Thietane
Other names
Thiacyclobutane
Trimethylene sulfide
Identifiers
3D model (JSmol)
102383
ChemSpider
ECHA InfoCard 100.005.469 Edit this at Wikidata
EC Number
  • 206-015-0
UN number 1993
  • InChI=1S/C3H6S/c1-2-4-3-1/h1-3H2 checkY
    Key: XSROQCDVUIHRSI-UHFFFAOYSA-N checkY
  • C1CSC1
Properties
C3H6S
Molar mass 74.14 g·mol−1
Appearance Colourless liquid
Odor Sulfurous
Density 1.028 g cm-3
Hazards
GHS labelling:
GHS02: Flammable GHS07: Exclamation mark
Danger
H225, H302
P210
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
2
4
1
Flash point -11(9) °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Thietane is a heterocyclic compound containing a saturated four-membered ring with three carbon atoms and one sulfur atom.[1][2]

References

  1. ^ Leśniak, S (2008). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry III. 2.07: 389–428. doi:10.1016/B978-008044992-0.00207-8. {{cite journal}}: Cite has empty unknown parameter: |1= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
  2. ^ Block, E (1996). "Thietanes and Thietes: Monocyclic". Comprehensive Heterocyclic Chemistry II. 1.24: 773–802. doi:10.1016/B978-008096518-5.00024-1. {{cite journal}}: Cite has empty unknown parameter: |1= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)