Phenyl methylcarbamates
Phenyl Methylcarbamates are a class of carbamate compounds derived from phenol and methanol, which have found extensive applications in the pesticide industry due to their potent insecticidal properties. These chemicals exhibit excellent stability under various environmental conditions, making them suitable for use in both agricultural and non-agricultural settings. They are typically formulated into emulsifiable concentrates or wettable powders for easy application via spraying. Additionally, phenyl methylcarbamates demonstrate low toxicity towards mammals while being highly effective against a wide range of pests, contributing to their widespread adoption in pest management strategies. The compounds undergo hydrolysis under acidic conditions, leading to the release of toxic metabolites that contribute to their insecticidal action. Due to their balanced safety profile and efficacy, phenyl methylcarbamates continue to be an important component in modern integrated pest management programs.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Carbamic acid,N-methyl-, 2-chlorophenyl ester | 3942-54-9 | C8H8ClNO2 |
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Phenol,2-(2-chloro-1-methoxyethoxy)-, 1-(N-methylcarbamate) | 51487-69-5 | C11H14ClNO4 |
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Benzoic acid,4-[[(methylamino)carbonyl]oxy]-, methyl ester | 21998-12-9 | C10H11NO4 |
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Phenol,2-methyl-5-(1-methylethyl)-, 1-(N-methylcarbamate) | 2752-71-8 | C12H17NO2 |
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Formetanate-d6, Hydrochloride | 1185240-24-7 | C11H16ClN3O2 |
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2655-03-0 | C12H16ClNO2 | |
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2-(trichloromethyl)phenyl methylcarbamate | 716-27-8 | C9H8Cl3NO2 |
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Metolcarb | 1129-41-5 | C9H11NO2 |
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| 17795-78-7 | C13H17ClN2O3 |
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Ethiofencarb Sulfone | 53380-23-7 | C11H15NO4S |
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