| Identification | Back Directory | [Name]
3,4-dichlorobenzyl methylcarbamate | [CAS]
1966-58-1 | [Synonyms]
UC-22463
3,4-Sirmate
3,4-Dichlormate
3,4-dichlorobenzyl methylcarbamate
3,4-dichlorobenzyl N-methylcarbamate
N-Methylcarbamic acid 3,4-dichlorobenzyl ester
Benzenemethanol, 3,4-dichloro-, 1-(N-methylcarbamate) | [EINECS(EC#)]
217-813-3 | [Molecular Formula]
C9H9Cl2NO2 | [MOL File]
1966-58-1.mol | [Molecular Weight]
234.08 |
| Hazard Information | Back Directory | [Production Methods]
Dichlormate was commercially produced via a carbamate esterification process. The synthesis typically involved reacting 3,4-dichlorobenzyl alcohol with methyl isocyanate or methylcarbamoyl chloride under controlled conditions to form the N-methylcarbamate ester. This reaction was carried out in an organic solvent with a catalyst or base to facilitate ester formation. After completion, the crude product was purified through recrystallisation or distillation to obtain technical-grade dichlormate. | [Mechanism of action]
Thought to be due to inhibition of the synthesis of carotenoids and to the consequent photodestruction of chlorophyll and chloroplast disruption | [Pesticide Type]
Herbicide |
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