Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester

Base Information

• Chemical Name: Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester
• CAS No.: 2286-43-3
• Molecular Formula: C8H4F4O2
• Molecular Weight: 208.112
• DSSTox Substance ID: DTXSID90444717
• Nikkaji Number: J705.792J
• Wikidata: Q82262958
• Mol file: 2286-43-3.mol

Synonyms:Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester;2286-43-3;SCHEMBL12704880;DTXSID90444717;MOZMNRLVKQNXPR-UHFFFAOYSA-N;Fluoroformic acid 4-(trifluoromethyl)phenyl ester

Chemical Property of Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester

Chemical Property:

• XLogP3: 3.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 208.01474201
• Heavy Atom Count: 14
• Complexity: 206

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1C(F)(F)F)OC(=O)F

Technology Process of Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester

There total 2 articles about Carbonofluoridic acid, 4-(trifluoromethyl)phenyl ester 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:

C11H13F3O2Si → p-Trifluormethylphenoxy-carbonylfluorid (2286-43-3) + 4-trifluoromethyl-benzoyl fluoride (368-94-5)

Guidance literature:

With xenon difluoride; In various solvent(s); for 3h; Yield given. Yields of byproduct given; Ambient temperature;

DOI:10.1039/p19960000121

Reference yield:

→ p-Trifluormethylphenoxy-carbonylfluorid (2286-43-3)

Guidance literature:

4-Trifluormethylphenol, COFCl, Toluol, Tributylamin;

Reference yield:

p-Trifluormethylphenoxy-carbonylfluorid (2286-43-3) + N-butylamine (109-73-9,85404-21-3) → p-trifluoromethylphenyl-N-butylcarbamate (167698-12-6)

Guidance literature:

With triethylamine; In xylene;

Downstream raw materials:

p-trifluoromethylphenyl-N-butylcarbamate

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