| Weight | 118.161 g/mol |
|---|---|
| Formula | C3H6N2OS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
N-Acetylthiourea (591-08-2)
1-acetylthiourea · acetylthiourea sodium salt · acetylthiourea
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- OxyhalogenSulfur Chemistry: Kinetics and Mechanism of Oxidation of N-Acetylthiourea by Chlorite and Chlorine Dioxide1 (Journal of Physical Chemistry A, 2006)
- Infrared Spectra and Conformation of N-Acetylthiourea (Bulletin of the Chemical Society of Japan, 1982)
- The mechanism of thermal elimination of urea and thiourea derivatives. Part 1. Rate data for pyrolysis of N-acetylurea, N-acetylthiourea, N,N -diacetylthiourea, and N-acetylthiobenzamide (Heteroatom Chemistry, 1996)
- N-Phenyl-N-acetylthioureaa specific reagent for photometric determination of ruthenium (Talanta, 1982)
- Formation and structure elucidation of N-(2,3,4-tri-O-acetyl--d-glucopyranosyl)-N-acetylthiourea (Carbohydrate Research, 2009)
- The SN mechanism in aromatic compounds. Part XXXIX. Halogen mobility and reagent strength in reactions of some heavy atom neutral nucleophiles (thiourea, N-acetylthiourea, and selenourea) with 1-chloro- and 1-fluoro-2,4-dinitrobenzenes (Journal of The Chemical Society-perkin Transactions 1, 1972)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-acetylthiourea
- acetylthiourea sodium salt
- acetylthiourea
-
SMILESCC(=O)NC(=S)N
-
InChIKeyIPCRBOOJBPETMF-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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(6610-31-7)
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cyclopropylurea
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N-Acetylthiourea
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