| Weight | 131.156 g/mol |
|---|---|
| Formula | C4H5NO2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Ethoxycarbonyl isothiocyanate (16182-04-0)
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- Friedel-Crafts thioacylation with ethoxycarbonyl isothiocyanate. One-step synthesis of aromatic thioamides (Journal of Organic Chemistry, 1976)
- Structure of Bis(triphenylphosphine)(N-ethoxycarbonyldithiocarbimato)palladium(II), Formed by the Reaction of Excess Ethoxycarbonyl Isothiocyanate with Palladium(0) in the Presence of Triphenylphosphine (Inorganic Chemistry, 1977)
- Addition-cyclisations of ethoxycarbonyl isothiocyanate with hydrazine derivatives as a source of thiadiazoles and triazoles (Journal of Heterocyclic Chemistry, 1989)
- Chemistry of amidrazonesIV : Addition-cyclisation of amidrazones with isocyanate esters and ethoxycarbonyl isothiocyanate (Tetrahedron, 1976)
- Recent advances in the chemistry of ethoxycarbonyl isothiocyanate and related compounds (Journal of Heterocyclic Chemistry, 1983)
- Chemistry of biureasII: Synthesis and cyclisation of thiobiureas derived from (thio)carbonohydrazides and ethoxycarbonyl isothiocyanate (Tetrahedron, 1977)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)N=C=S
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InChIKeyBDTDECDAHYOJRO-UHFFFAOYSA-N
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Synthesis
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Ethoxycarbonyl isothiocyanate
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