| Weight | 114.104 g/mol |
|---|---|
| Formula | C4H6N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
5-Methylhydantoin (616-03-5)
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- Repair and coding properties of 5-hydroxy-5-methylhydantoin nucleosides inserted into DNA oligomers. (Chemical Research in Toxicology, 2000)
- Preferential crystallisation and comparative crystal growth study between pure enantiomer and racemic mixture of a chiral molecule: 5-ethyl-5-methylhydantoin (Chemical Engineering Science, 2001)
- Oscillating crystallization in solution between (+)- and (-)-5-ethyl-5-methylhydantoin under the influence of stirring (Journal of Physical Chemistry B, 2002)
- Enzymatic production of L-tryptophan from DL-5-indolylmethylhydantion. I. Enzymatic production of L-tryptophan from L- and DL-5-indolyl-methylhydantoin by newly isolated bacterium. (Agricultural and biological chemistry, 1977)
- The antiviral compound 5-(3,4-dichlorophenyl) methylhydantoin inhibits the post-synthetic cleavages and the assembly of poliovirus in a cell-free system (Antiviral Research, 2000)
- Combined Effect of Polymorphism and Process on Preferential Crystallization: Example with ()-5(4-Methylphenyl)-5-methylhydantoin (Organic Process Research & Development, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1C(=O)NC(=O)N1
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InChIKeyVMAQYKGITHDWKL-UHFFFAOYSA-N
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