Fentrifanil

Base Information

• Chemical Name: Fentrifanil
• CAS No.: 62441-54-7
• Molecular Formula: C14H6 Cl F6 N3 O4
• Molecular Weight: 429.663
• Hs Code.: 2921440000
• European Community (EC) Number: 263-546-0
• UNII: SRS24TLG5G
• DSSTox Substance ID: DTXSID0040331
• Metabolomics Workbench ID: 143681
• Nikkaji Number: J18.826C
• Wikidata: Q27289357
• Mol file: 62441-54-7.mol

Synonyms:2'-chloro-2,4-dinitro-5'-6-di(trifluoromethyl)diphenylamine;CDTD;fentrifanil;N-(2-chloro-5-(trifluoromethyl)phenyl)-2,4-dinitro-6-(trifluoromethyl)benzenamine

Chemical Property of Fentrifanil

Chemical Property:

• Vapor Pressure: 9.72E-06mmHg at 25°C
• Boiling Point: 372.3°C at 760 mmHg
• PKA: -9.59±0.50(Predicted)
• Flash Point: 179°C
• PSA: 103.67000
• Density: 1.664g/cm³
• LogP: 7.05700
• XLogP3: 6.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 2
• Exact Mass: 428.9951023
• Heavy Atom Count: 28
• Complexity: 594

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1C(F)(F)F)NC2=C(C=C(C=C2[N+](=O)[O-])[N+](=O)[O-])C(F)(F)F)Cl
• Uses: Fluofenamine is an acaricide used in mites control. A pesticide.

Technology Process of Fentrifanil

There total 1 articles about Fentrifanil 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:

1-chloro-2,4-dinitro-6-trifluoromethylbenzene (392-95-0) + 3-amino-4-chlorobenzotrifluoride (121-50-6) → 2-chloro-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-benzenamine (62441-54-7)

Guidance literature:

With potassium hydroxide; In N-methyl-acetamide;

Reference yield:

2-chloro-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-benzenamine (62441-54-7) + diethoxyoxyphosphoranesulfenyl chloride → S-[N-[2-chloro-5-(trifluoromethyl)phenyl]-2,4-dinitro-6-(trifluoomethyl)phenyl]amino]-o,o-diethylphosphorothioic acid + S-[N-[2-Chloro-5-(trifluoromethyl)phenyl]-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]amino]-o,o-diethylphosphorothioic acid (83909-25-5)

Guidance literature:

In tetrahydrofuran;

Reference yield:

2-chloro-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-benzenamine (62441-54-7) + N-chlorothio-N-methyl-4-toluenesulphonamide (52913-45-8) → N-[N-[2-chloro-5-(trifluoromethyl)phenyl]-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]aminothio]-N-4-dimethylbenzenesulfonamide (75507-78-7)

Guidance literature:

In tetrahydrofuran; water;

upstream raw materials:

1-chloro-2,4-dinitro-6-trifluoromethylbenzene

3-amino-4-chlorobenzotrifluoride

Downstream raw materials:

S-[N-[2-Chloro-5-(trifluoromethyl)phenyl]-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]amino]-o,o-diethylphosphorothioic acid

N-[N-[2-chloro-5-(trifluoromethyl)phenyl]-N-[2,4-dinitro-6-(trifluoromethyl)phenyl]aminothio]-N-4-dimethylbenzenesulfonamide

Refernces