N-[2-(Trifluoromethyl)phenyl]benzenecarboximidoyl chloride

Base Information

Chemical Name:N-[2-(Trifluoromethyl)phenyl]benzenecarboximidoyl chloride
CAS No.:64321-99-9
Molecular Formula:C14H9ClF3N
Molecular Weight:283.68
Hs Code.:
DSSTox Substance ID:DTXSID80557224
Nikkaji Number:J450.161F

Synonyms:N-[2-(Trifluoromethyl)phenyl]benzenecarboximidoyl chloride;64321-99-9;SCHEMBL11375370;DTXSID80557224;RHGJCYWYCKTBAG-UYRXBGFRSA-N;N-(2-trifluoromethylphenyl)-benzimidoyl chloride;N-(2-trifluoromethylphenyl)-benzenecarboximidoyl chloride

Suppliers and Price of N-[2-(Trifluoromethyl)phenyl]benzenecarboximidoyl chloride

Supply Marketing:

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

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Chemical Property of N-[2-(Trifluoromethyl)phenyl]benzenecarboximidoyl chloride

Chemical Property:

XLogP3:5.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:283.0375615
Heavy Atom Count:19
Complexity:321

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=NC2=CC=CC=C2C(F)(F)F)Cl

Technology Process of N-[2-(Trifluoromethyl)phenyl]benzenecarboximidoyl chloride

There total 3 articles about N-[2-(Trifluoromethyl)phenyl]benzenecarboximidoyl chloride 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:

: 2946-71-6
N-<2-(trifluoromethyl)phenyl>benzamide

: 64321-99-9
N-(2-Trifluoromethyl-phenyl)-benzimidoyl chloride

Guidance literature:: With phosphorus pentachloride; In benzene; at 50 ℃; for 0.25h;

Reference yield:

: 88-17-5
2-(trifluoromethyl)benzenamine

: 64321-99-9
N-(2-Trifluoromethyl-phenyl)-benzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 12 h / 0 - 20 °C

2: thionyl chloride / 4 h / 80 °C

With thionyl chloride; triethylamine; In tetrahydrofuran;
DOI:10.1021/acs.joc.0c00833

Reference yield:

: 98-88-4
benzoyl chloride

: 64321-99-9
N-(2-Trifluoromethyl-phenyl)-benzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 12 h / 0 - 20 °C

2: thionyl chloride / 4 h / 80 °C

With thionyl chloride; triethylamine; In tetrahydrofuran;
DOI:10.1021/acs.joc.0c00833