Ethylene episulfoxide
Names | |
---|---|
Preferred IUPAC name 1λ4-Thiiran-1-one | |
Other names Ethylene sulfoxide Thiirane S-oxide Thiirane oxide | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChemSpider |
|
PubChem CID |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C2H4OS |
Molar mass | 76.11 g·mol−1 |
Appearance | colorless liquid |
Boiling point | 45–47 °C (113–117 °F; 318–320 K) 2 mm Hg |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Ethylene episulfoxide is the organosulfur compound with the formula C2H4SO. A colorless liquid, it is one of the simplest sulfoxides. Because it is a strained ring, ethylene sulfoxide is a highly reactive molecule, decomposing thermally to sulfur monoxide and ethylene. It is prepared by oxidation of ethylene sulfide with periodate.[1]
References
- ^ Hartzell, G. E.; Paige, Janet N. (1966). "Ethylene Episulfoxide". Journal of the American Chemical Society. 88: 2616–2617. doi:10.1021/ja00963a063.
- v
- t
- e
Sulfur compounds
disulfides
- Al2S3
- As2S2
- As2S3
- As2S5
- As4S4
- Au2S
- Au2S3
- B2S3
- BaS
- BeS
- Bi2S3
- CS2
- C3S2
- C6S6
- CaS
- CdS
- CeS
- CoS
- Cr2S3
- CSSe
- CSTe
- CuFeS2
- CuS
- D2S
- Dy2S3
- Er2S3
- EuS
- FeS2
- GaS
- H2S
- HfS2
- HgS
- In2S3
- K2S
- LaS
- LiS
- MgS
- MoS2
- MoS3
- NaHS
- Na2S
- NH4HS
- NiS
- P4Sx
- PbS
- PbS2
- PSCl3
- PSI3
- PtS
- ReS2
- Re2S7
- SiS
- SrS
- TlS
- VS
- SeS2
- S2U
- WS2
- WS3
- Sb2S3
- Sb2S5
- Sb4S3O3
- Sm2S3
- Y2S3
- ZrS2
- La
2O
2S - Gd
2O
2S
- S2Br2
- SBr2
- S2Cl2
- SCl2
- SCl4
- SF2
- SF4
- S2F10
- SF6
- S2I2
and oxyhalides
- SO2
- SO3
- SOBr2
- SOCl2
- SOF2
- SOF4
- H2S3O6
- H2SO3
- H2SO4
- H2S2O7
- H2SO5
Sulfites |
|
---|---|
Sulfates |
|
- C2H4S
- C2H6S3
- C4H4S
- C32H66S2
- CHCl3S
- C2H3SN