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| | DU 19892 Basic information |
| Product Name: | DU 19892 | | Synonyms: | DU 19892;1-(4-chlorophenyl)-3-(2,6-dichlorobenzoyl)urea;2,6-dichloro-N-[[(4-chlorophenyl)amino]carbonyl]-Benzamide PH 60-38 N-(2,6-Dichlorobenzoyl)-N-(4-chlorophenyl) urea 2,6-dichloro-n-(((4-chlorophenyl)amino)carbonyl)-benzamid 2,6-dichloro-n-(((4-chlorophenyl)amino)carbonyl)benzamide;2,6-Dichloro-N-[[(4-chlorophenyl)amino]carbonyl]benzamide;PH-60-38;Ai3-29053;Benzamide, 2,6-dichloro-N-(((4-chlorophenyl)amino)carbonyl)-;Brn 2819143 | | CAS: | 35409-97-3 | | MF: | C14H9Cl3N2O2 | | MW: | 343.59 | | EINECS: | | | Product Categories: | | | Mol File: | 35409-97-3.mol |  |
| | DU 19892 Chemical Properties |
| density | 1.516±0.06 g/cm3(Predicted) | | pka | 9.08±0.46(Predicted) |
| | DU 19892 Usage And Synthesis |
| Production Methods | Public sources do not provide a published industrial synthesis for 1 (4 chlorophenyl) 3 (2,6 dichlorobenzoyl)urea, but its production can be described based on standard benzoylurea chemistry and its chemical structural. It would have been produced by first preparing the 2,6 dichlorobenzoyl chloride intermediate from the corresponding acid, followed by reaction with 4 chloroaniline to form a substituted benzamide. This benzamide is then converted into the final benzoylurea through controlled phosgene type carbamoylation or by using safer phosgene substitutes, yielding the urea linkage characteristic of this insecticide family. | | Mechanism of action | Chitin synthesis inhibitor | | Pesticide Type | Insecticide; Insect Growth Regulator |
| | DU 19892 Preparation Products And Raw materials |
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