Phenol, 4-(phenylmethyl)-, 1-carbamate, commonly known as phenylcarbamate, is an organic compound characterized by its phenolic structure combined with a carbamate functional group. It features a phenylmethyl group (benzyl) attached to the para position of the phenolic ring, which contributes to its chemical properties. This compound is typically a white to off-white solid and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the aromatic rings. It exhibits moderate stability under standard conditions but can undergo hydrolysis in the presence of strong acids or bases, leading to the release of phenol and the corresponding amine. Phenylcarbamate is often studied for its potential applications in pharmaceuticals and agrochemicals, as well as its role in various chemical syntheses. Safety considerations include its potential toxicity and the need for proper handling to avoid exposure. Overall, its unique structure and properties make it a subject of interest in both industrial and research settings.

Phenol, 4-(phenylmethyl)-, 1-carbamate

101-71-3: Phenol, 4-(phenylmethyl)-, 1-carbamate, Carbamic acid, α-phenyl-p-tolyl ester, p-Benzylphenyl carbamate, p-Cresol, α-phenyl-, carbamate, Phenol, 4-(phenylmethyl)-, carbamate

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CAS 101-71-3: Phenol, 4-(phenylmethyl)-, 1-carbamate

Diphenan

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