| Weight | 197.215 g/mol |
|---|---|
| Formula | C8H7NO3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Tosyl isocyanate (4083-64-1)
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- A Highly Efficient Synthesis of ()-PI-091 Construction of the 4-Alkoxy-2-butene-4-lactam Skeleton from Fischer-Type Carbene Complexes, Alkynyllithiums, and Tosyl Isocyanate (Journal of Organic Chemistry, 1997)
- Regioselective reactions of -aminovinyl trifluoromethyl ketones with tosyl isocyanate (Tetrahedron, 2003)
- Ruthenium Complex-Catalyzed Domino Addition/exo- Cycloisomerization of Propargylic Alcohols and Tosyl Isocyanate to Form Oxazolidinones (Advanced Synthesis & Catalysis, 2015)
- Regioselective reactions of N-monosubstituted -aminovinyl trifluoromethyl ketones with tosyl isocyanate (Tetrahedron Letters, 2000)
- Reaction of 1-trimethylsilyl-1,4-dihydropyridine with ethyl azidoformate and p-tosyl isocyanate (Journal of Organic Chemistry, 1969)
- Synthesis of 2-Imino-3,4-dihydro-2H-benzoxa(thia)zolo[3,2-a]-1,3,5-triazin-4-ones(thiones) by Reaction of Benzoxa(thia)zolyl-2-guanidines with Tosyl Isocyanate and Phenyl Isothiocyanate (Chemistry of Heterocyclic Compounds, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H315: Causes skin irritation
Warning Skin corrosion/irritation - Category 2 - H334: May cause allergy or asthma symptoms or breathing difficulties if inhaled
Danger Sensitization, respiratory - Category 1 -
SMILESCC1=CC=C(C=C1)S(=O)(=O)N=C=O
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InChIKeyVLJQDHDVZJXNQL-UHFFFAOYSA-N
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Tosyl isocyanate
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