| Weight | 118.157 g/mol |
|---|---|
| Formula | C4H6O2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
3-Sulfolene (77-79-2)
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- Sigma-Aldrich - 3-Sulfolene22.50 - 53.40 USD
- Fisher Scientific - Search for 3-Sulfolene
- TCI - 3-Sulfolene14.00 - 52.00 USD
- Lithium aluminium hydride promoted extrusion of SO2 from sulfolenes and sulfolene-adducts. 1,3-dienes, 3-chloro- and 3,3-dichloro-1,4-dienes and skipped polyenes (Tetrahedron Letters, 1977)
- Preparation of (phenyloxazolo)-3-sulfolene. A precursor for (phenyloxazolo)-o-quinodimethane (Journal of Organic Chemistry, 1994)
- Synthesis of furan-fused 3-sulfolene. A stable precursor to furan analogue of o-quinodimethane (Heterocycles, 1992)
- Regioselective alkylation of 3-trimethylsilyl-3-sulfolene: route to stereospecific 2-silylated butadiene derivatives (Journal of Organic Chemistry, 1988)
- Studies in alkylation of 3-methyl-3-sulfolene and thermolysis of resulting 2-alkyl-3-sulfolenes: Convenient synthesis of 1,2-disubstituted-1,3-dienes (Tetrahedron, 1992)
- Synthesis of ()-Lupinine and ()-Epi-lupinine using Regioselective Alkylation of Functionalized 3-Sulfolene (Heterocycles, 1985)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C=CCS1(=O)=O
-
InChIKeyMBDNRNMVTZADMQ-UHFFFAOYSA-N
- Pubchem - 3-Sulfolene
- Wikipedia - 3-sulfolene
Sulfolene, or butadiene sulfone is a cyclic organic chemical with a sulfone functional group. It is the product of a (4+1) cycloaddition (or more technically a cheletropic reaction) between butadiene and sulfur dioxide. Catalytic hydrogenation yields sulfolane, a solvent used in the petrochemical industry for the extraction of aromatics from hydrocarbon streams.
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