| Weight | 151.165 g/mol |
|---|---|
| Formula | C8H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
PHENYL METHYLCARBAMATE (1943-79-9)
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- Metabolism of two acaricidal chemicals, N'-(4-chloro-o-tolyl)-N,N-dimethylformamidine chlorphenamidine) and m-[[(dimethylamino)methylene]amino]phenyl methylcarbamate hydrochloride (formetanate). (Journal of Agricultural and Food Chemistry, 1970)
- Highly efficient intramolecular nucleophilic reactions. The cyclization of p-nitrophenyl N-(2-mercaptophenyl)-N-methylcarbamate and phenyl N-(2-aminophenyl)-N-methylcarbamate (Journal of the American Chemical Society, 1975)
- Possible role of tyrosinase and cytochrome P-450 in the metabolism of 1-naphthyl methylcarbamate (carbaryl) and phenyl methylcarbamate by houseflies. (Journal of Agricultural and Food Chemistry, 1969)
- Quantitative structure-activity relationship of phenyl N-methylcarbamate inhibition of acetylcholinesterase. (Journal of Agricultural and Food Chemistry, 1981)
- Metabolites and photoproducts of 3-(2-butyl)phenyl N-methylcarbamate and N-benzenesulfenyl-N-methylcarbamate (Journal of Agricultural and Food Chemistry, 1973)
- Antileukemic activity of derivatives of 1-phenyl-2,5-dimethyl-3,4-bis(hydroxymethyl)pyrrole bis(N-methylcarbamate). (Journal of Medicinal Chemistry, 1977)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCNC(=O)OC1=CC=CC=C1
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InChIKeySCWKRWCUMCMVPW-UHFFFAOYSA-N
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