| Weight | 116.145 g/mol |
|---|---|
| Formula | C3H4N2OS |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Pseudothiohydantoin (556-90-1)
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- Donor properties of thiohydantoin and pseudothiohydantoin towards cobalt(II) and nickel(II) salts (Australian Journal of Chemistry, 1976)
- Syntheses and characterization of 5-substituted hydantoins and thiazolinesimplications for crystal engineering of hydrogen bonded assemblies. Crystal structures of 5-(2-pyridylmethylene)hydantoin, 5-(2-pyridylmethylene)-2-thiohydantoin, 5-(2-pyridylmethylene)thiazolidine-2,4-dione, 5-(2-pyridylmethylene)rhodanine and 5-(2-pyridylmethylene)pseudothiohydantoin (Journal of The Chemical Society-perkin Transactions 1, 2000)
- Heterocyclic tautomerism. VI. A redetermination and reassignment of the structure of 2aminothiazol4(5H)one (pseudothiohydantoin) (Acta Crystallographica Section C-crystal Structure Communications, 1994)
- Pseudothiohydantoin complexes of NiII halides and perchlorate (Inorganica Chimica Acta, 1973)
- Condensation of pseudothiohydantoin with substituted isatins (Russian Journal of General Chemistry, 2011)
- Pseudothiohydantoin-protein, derivatives, and solutions therefrom (1944)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(=O)N=C(S1)N
-
InChIKeyHYMJHROUVPWYNQ-UHFFFAOYSA-N
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