| Identification | Back Directory | [Name]
5-chloro-2-[4-chloro-2-[(3,4-dichlorophenyl)carbamoylamino]phenoxy]ben zenesulfonic acid | [CAS]
24019-05-4 | [Synonyms]
N-(3,4-Dichlorophenyl)-N'-[2-(4-chloro-2-sulfophenoxy)-5-chlorophenyl]urea
5-chloro-2-[4-chloro-2-[(3,4-dichlorophenyl)carbamoylamino]phenoxy]ben zenesulfonic acid
Benzenesulfonic acid, 5-chloro-2-[4-chloro-2-[[[(3,4-dichlorophenyl)amino]carbonyl]amino]phenoxy]- | [Molecular Formula]
C19H12Cl4N2O5S | [MDL Number]
MFCD30580414 | [MOL File]
24019-05-4.mol | [Molecular Weight]
522.19 |
| Hazard Information | Back Directory | [Definition]
ChEBI: An organochlorine pesticide consisting of 1,3-diphenylurea having chloro substituents at the 3-, 4- and 5'-positions and a 4-chloro-2-sulfophenoxy group at the 2'-position. | [Production Methods]
Sulcofuron is commercially synthesised through a multi-step process that constructs its complex sulfonylurea structure. The synthesis typically begins with the preparation of 4,4'-dichloro-2-nitrodiphenyl ether, formed by reacting p-chlorophenol with 2,5-dichloronitrobenzene in the presence of potassium hydroxide at elevated temperatures. This intermediate is then subjected to further transformations including reduction, urea formation, and sulfonation to yield the final active ingredient. | [Mechanism of action]
Inhibits the synthesis of the enzyme required to break down keratin | [Pesticide Type]
Insecticide |
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