Weight | 60.121 g/mol |
---|---|
Formula | C2H4S |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Thiirane (420-12-2)
ethylene sulfide · divinyl sulfide · divinylsulfide
Score:
#1107 in Physics
,
#3155 in Chemistry
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- The Microwave Spectra, Structure, and Dipole Moments of Ethylene Oxide and Ethylene Sulfide (Journal of Chemical Physics, 1951)
- New Synthetic Methodologies for Amphiphilic Multiblock Copolymers of Ethylene Glycol and Propylene Sulfide (Macromolecules, 2001)
- Reactions of aziridine, thiirane, and oxirane with isocyanide ligands in complexes of palladium(II) and platinum(II): syntheses of neutral five-membered cyclic diamino-, aminothio-, and aminooxycarbene compounds (Inorganic Chemistry, 1988)
- Addition of selenium dibromide to divinyl sulfide: spontaneous rearrangement of 2,6-dibromo-1,4-thiaselenane to 5-bromo-2-bromomethyl-1,3-thiaselenolane (Tetrahedron Letters, 2009)
- Inhibition of aromatase cytochrome P-450 by 10-oxirane and 10-thiirane substituted androgens. Implications for the structure of the active site. (Journal of Biological Chemistry, 1987)
- Thermodynamic Properties and Ideal-Gas Enthalpies of Formation for Dicyclohexyl Sulfide, Diethylenetriamine, Di-n-octyl Sulfide, Dimethyl Carbonate, Piperazine, Hexachloroprop-1-ene, Tetrakis(dimethylamino)ethylene, N,N-Bis-(2-hydroxyethyl)ethylenediamine, and 1,2,4-Triazolo[1,5-a]pyrimidine (Journal of Chemical & Engineering Data, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H225: Highly Flammable liquid and vapor
Danger Flammable liquids - Category 2 - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B - H370: Causes damage to organs
Danger Specific target organ toxicity, single exposure - Category 1 - ethylene sulfide
- divinyl sulfide
- divinylsulfide
-
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- Pubchem - Thiirane
- Wikipedia - ethylene sulfide
Thiirane, more commonly known as ethylene sulfide, is the cyclic chemical compound with the formula C2H4S. It is the smallest sulfur-containing heterocycle and the simplest episulfide. Like many organosulfur compounds, this species has a stench.
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