The kinetics of hydrolysis of the carbamoyl group in salicylanilide N-methylcarbamate (I) and 4-biphenylyl N-methylcarbamate (11) showed that the reaction was first order with respect to both hydroxide ion and carbamate. At 37", the hydroxideion-catalyzed hydrolysis of 1 to yield salicylanilide (111
β¦ LIBER β¦
In vitro and in vivo hydrolysis of 4-benzoylphenyl N-methylcarbamate
β Scribed by Leo W. Brown; Arlington A. Forist
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 235 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0022-3549
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