| Weight | 181.216 g/mol |
|---|---|
| Formula | C8H7NO2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Tosyl cyanide (19158-51-1)
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- Mild CobaltCatalyzed Hydrocyanation of Olefins with Tosyl Cyanide (Angewandte Chemie, 2007)
- On the Preparation of Aryl Nitriles Using Tosyl Cyanide (Journal of Organic Chemistry, 1995)
- Preparation of novel 1,2,4-thiadiazoles by cyclization with 4-methylbenzenesulfonyl cyanide (tosyl cyanide) (Journal of Heterocyclic Chemistry, 1993)
- A novel sulfinylation of alkenes by tosyl cyanide with titanium(IV) chloride (Tetrahedron Letters, 1999)
- Unusual mechanism of hydrolysis of the tosyl cyanidecyclopentadiene adduct to the lactam 2-azabicyclo[2.2.1]hept-5-en-3-one (Chemical Communications, 1996)
- Thermal addition of tosyl cyanide to norbornadiene. A HomoDielsAlder cycloaddition versus homoconjugate 1,4addition (Recueil des Travaux Chimiques des Pays-Bas, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=C(C=C1)S(=O)(=O)C#N
-
InChIKeyJONIMGVUGJVFQD-UHFFFAOYSA-N
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Tosyl cyanide
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