73265-15-3

Basic information

• Product Name: 3,5-Dichloro-4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)aniline
• Synonyms: 3,5-Dichloro-4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)aniline
• CAS NO: 73265-15-3
• Molecular Formula: C12H6Cl3F3N2O
• Molecular Weight: 357.55
• Mol File: 73265-15-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 143～146℃
• Appearance: /
• CAS DataBase Reference: 3,5-Dichloro-4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dichloro-4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)aniline(73265-15-3)
• EPA Substance Registry System: 3,5-Dichloro-4-(3-chloro-5-trifluoromethyl-2-pyridyloxy)aniline(73265-15-3)

Safety Data

• Hazardous Substances Data: 73265-15-3(Hazardous Substances Data)

Upstream product

• 5930-28-9 4-amino-2,6-dichlorophenol 
• 69045-84-7 2,3-dichloro-5-trifluoromethylpyridine 
• 108-99-6 3-Methylpyridine 
• 69045-78-9 2-chloro-5-(Trichloromethyl)-pyridine 
• 69045-83-6 2,3-dichloro-5-(trichloromethyl)pyridine 
• 100-02-7 4-nitro-phenol 
• 618-80-4 2,6-dichloro-4-nitrophenol 

Relevant articles and documents

Synthesis method of chlorfluazuron and application of chlorfluazuron in insecticide preparation

The invention belongs to the technical field of pesticide preparations, particularly relates to a synthesis method of chlorfluazuron and further discloses an application of chlorfluazuron in insecticide preparation. According to the synthesis method of chlorfluazuron, chlorfluazuron is prepared from 2,3-dichloro-5-(trifluoromethyl)pyridine, 2,6-dichloro-4-aminophenol and 2,6-difluorobenzoyl isocyanate as synthetic raw materials and N,N-dimethylacetamide as a reaction solvent on the basis of a conventional synthesis route in the prior art; under the action of a ZSM molecular sieve based catalyst, not only can synthesis of chlorfluazuron be realized, but also a reaction can be performed with the same reaction solvent, so that the problem of complicated process caused by the fact that solvents are required to be recovered step by step during two-step synthesis of chlorfluazuron in the prior art is solved; compared with the technology in the prior art, the synthesis method of chlorfluazuron has the advantages that the synthesis yield of products is further increased and product content is higher.