(4-Methylphenyl) 4-fluorobenzoate

Base Information

Chemical Name:(4-Methylphenyl) 4-fluorobenzoate
CAS No.:32792-48-6
Molecular Formula:C14H11FO2
Molecular Weight:230.239
Hs Code.:
DSSTox Substance ID:DTXSID10357279
Wikidata:Q82137136
Mol file:32792-48-6.mol

Synonyms:(4-methylphenyl) 4-fluorobenzoate;32792-48-6;4-methylphenyl 4-fluorobenzoate;SCHEMBL533392;DTXSID10357279;4-fluoro-benzoic acid p-tolyl ester;AKOS003498204;AO-548/41238333

Suppliers and Price of (4-Methylphenyl) 4-fluorobenzoate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of (4-Methylphenyl) 4-fluorobenzoate

Chemical Property:

PSA：26.30000
LogP:3.35330
XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:230.07430775
Heavy Atom Count:17
Complexity:251

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)OC(=O)C2=CC=C(C=C2)F

Technology Process of (4-Methylphenyl) 4-fluorobenzoate

There total 5 articles about (4-Methylphenyl) 4-fluorobenzoate 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:

: 530-46-1
4-fluoro-4'-methylbenzophenone

: 32792-41-9
4-methylbenzoic acid 4-fluorophenyl ester

: 32792-48-6
p-cresyl p-fluorobenzoate

Guidance literature:: With sulfuric acid; dihydrogen peroxide; acetic anhydride; acetic acid; for 4h; Title compound not separated from byproducts; Ambient temperature;
DOI:10.1016/0022-1139(93)02930-D

Reference yield:

: 106-44-5
p-cresol

: C₁₆H₁₄F₂N₂O₄

: 32792-48-6
p-cresyl p-fluorobenzoate

Guidance literature:: With zinc trifluoromethanesulfonate; potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 21h;
DOI:10.1002/adsc.201701646

Reference yield:

: 72755-09-0
4-fluoro-N-methoxybenzamide

: 32792-48-6
p-cresyl p-fluorobenzoate

Guidance literature:: Multi-step reaction with 2 steps

1: tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 3.5 h / 0 °C / Electrolysis

2: zinc trifluoromethanesulfonate; potassium carbonate / N,N-dimethyl-formamide / 21 h / 20 °C

With tetra-(n-butyl)ammonium iodide; zinc trifluoromethanesulfonate; potassium carbonate; In N,N-dimethyl-formamide;
DOI:10.1002/adsc.201701646