N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride

Base Information

Chemical Name:N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride
CAS No.:87228-18-0
Molecular Formula:C₈H₃Cl₂F₄N
Molecular Weight:260.018
Hs Code.:

Synonyms:N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride

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Technology Process of N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride

There total 1 articles about N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 56-23-5
tetrachloromethane

: 4127-63-3
4-CH3C6F4NH2

: 87228-18-0
N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride

Guidance literature:: With aluminium trichloride;
DOI:10.1016/S0022-1139(00)84039-7

Reference yield: 60.0%

: 64717-99-3
N-Pentafluorophenyltrichloroacetimidoyl chloride

: 87228-18-0
N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride

: 1-Pentafluorophenyl-3-(4'-methyl-2',3',5',6'-tetrafluorophenyl)-4,4,5,5-tetrachloro-2-imidazolidone

Guidance literature:: With aluminium trichloride; In Hexafluorobenzene; at 80 ℃; for 9h;
DOI:10.1016/S0022-1139(99)00257-2

Reference yield:

: 87228-18-0
N-(4-Methyl-2,3,5,6-tetrafluorophenyl)carbonimidoyl dichloride

: 103-49-1
dibenzylamine

: 20455-68-9
N,N-dibenzylamine hydrochloride

: C₂₂H₁₇ClF₄N₂

Guidance literature:: In acetonitrile; at 25 ℃; Rate constant; infl. of the var. (acceptor or donor ) substituents in phenyl ring of a substrate to the reaction rate;
DOI:10.1016/S0022-1139(00)83067-5