Thiirane

Thiirane
Skeletal formula of thiirane	Spacefill model of thiirane
Names
	Systematic IUPAC name Thiirane
	Other names 2,3-Dihydrothiirene; Ethylene sulfide; Thiacyclopropane
Identifiers
CAS Number	420-12-2 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	102379
ChEBI	CHEBI:30977 ;
ChemSpider	9481 ;
ECHA InfoCard	100.006.359
EC Number	206-993-9;
Gmelin Reference	1278
KEGG	C19419 ;
MeSH	ethylene+sulfide
PubChem CID	9865;
RTECS number	KX3500000;
UN number	1992
CompTox Dashboard (EPA)	DTXSID3049411 ;
	InChI InChI=1S/C2H4S/c1-2-3-1/h1-2H2 Key: VOVUARRWDCVURC-UHFFFAOYSA-N ;
	SMILES C1CS1;
Properties
Chemical formula	C2H4S
Molar mass	60.11 g·mol−1
Appearance	Pale, yellow liquid
Density	1.01 g cm−3
Melting point	−109 °C (−164 °F; 164 K)
Boiling point	56 °C; 133 °F; 329 K
Vapor pressure	28.6 kPa (at 20 °C)
Thermochemistry
Std enthalpy of; formation (ΔfH⦵298)	51-53 kJ mol−1
Std enthalpy of; combustion (ΔcH⦵298)	-2.0126 MJ mol−1
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H225, H301, H318, H331
Precautionary statements	P210, P261, P280, P301+P310, P305+P351+P338, P311
NFPA 704 (fire diamond)	3 4 2
Flash point	10 °C (50 °F; 283 K)
Related compounds
Related heterocycles	Ethylene oxide; Aziridine; Borirane
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Thiirane, more commonly known as ethylene sulfide, is the cyclic chemical compound with the formula C₂H₄S.^[2] It is the smallest sulfur-containing heterocycle and the simplest episulfide. Like many organosulfur compounds, this species has a stench. Thiirane is also used to describe any derivative of the parent ethylene sulfide.

Preparation

It is prepared by the reaction of ethylene carbonate and KSCN.^[3] For this purpose the KSCN is first melted under vacuum to remove water.

KSCN + C₂H₄O₂CO → KOCN + C₂H₄S + CO₂

Reactions

Ethylenesulfide adds to amines to afford 2-mercaptoethylamines,^[4] which are good chelating ligands.

C₂H₄S + R₂NH → R₂NCH₂CH₂SH

Dithiiranes

Dithiiranes are three membered rings containing two sulfur atoms and one carbon. One example was prepared by oxidation of a 1,3-dithietane.^[5]

References

^ ^a ^b ^c ^d "thiirane (CHEBI:30977)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.
^ Warren Chew; David N. Harpp (1993). "Recent aspects of thiirane chemistry". Journal of Sulfur Chemistry. 15 (1): 1–39. doi:10.1080/01961779308050628.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Searles, S.; Lutz, E. F.; Hays, H. R.; Mortensen, H. E. (1973). "Ethylene Sulfide". Organic Syntheses; Collected Volumes, vol. 5, p. 562.
^ R. J. Cremlyn “An Introduction to Organosulfur Chemistry” John Wiley and Sons: Chichester (1996). ISBN 0-471-95512-4.
^ Ahhiko Ishii, Masamatsu Hoshino, and Juzo Nakayama "Recent Advances in Chemistry of Dithiirane and Small Ring Compounds Containing Two Chalcogen Atoms" Pure & Appl. Chem., 1996, volume 68, pp. 869-874.doi:10.1002/chin.199650272

[thiirane_(CHEBI:30977)-1] "thiirane (CHEBI:30977)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute.

[2] Warren Chew; David N. Harpp (1993). "Recent aspects of thiirane chemistry". Journal of Sulfur Chemistry. 15 (1): 1–39. doi:10.1080/01961779308050628.{{cite journal}}: CS1 maint: multiple names: authors list (link)

[3] Searles, S.; Lutz, E. F.; Hays, H. R.; Mortensen, H. E. (1973). "Ethylene Sulfide". Organic Syntheses; Collected Volumes, vol. 5, p. 562.

[4] R. J. Cremlyn “An Introduction to Organosulfur Chemistry” John Wiley and Sons: Chichester (1996). ISBN 0-471-95512-4.

[5] Ahhiko Ishii, Masamatsu Hoshino, and Juzo Nakayama "Recent Advances in Chemistry of Dithiirane and Small Ring Compounds Containing Two Chalcogen Atoms" Pure & Appl. Chem., 1996, volume 68, pp. 869-874.doi:10.1002/chin.199650272

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