1-[2-(Benzoyloxy)-5-chloro-4-methylphenyl]ethanone

Base Information

Chemical Name:1-[2-(Benzoyloxy)-5-chloro-4-methylphenyl]ethanone
CAS No.:4010-27-9
Molecular Formula:C₁₆H₁₃ClO₃
Molecular Weight:288.73
Hs Code.:
DSSTox Substance ID:DTXSID901229551
Nikkaji Number:J479.319F

Synonyms:1-[2-(Benzoyloxy)-5-chloro-4-methylphenyl]ethanone;DTXSID901229551;4010-27-9

Suppliers and Price of 1-[2-(Benzoyloxy)-5-chloro-4-methylphenyl]ethanone

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
Packaging
price

Total 1 raw suppliers

Chemical Property of 1-[2-(Benzoyloxy)-5-chloro-4-methylphenyl]ethanone

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:288.0553220
Heavy Atom Count:20
Complexity:363

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=C(C=C1Cl)C(=O)C)OC(=O)C2=CC=CC=C2

Technology Process of 1-[2-(Benzoyloxy)-5-chloro-4-methylphenyl]ethanone

There total 1 articles about 1-[2-(Benzoyloxy)-5-chloro-4-methylphenyl]ethanone 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:

: 4010-27-9
Benzoic acid 2-acetyl-4-chloro-5-methyl-phenyl ester

Guidance literature:: a.d. 2-OH-Acetophenon, Acylierung;

Reference yield:

: 4010-27-9
Benzoic acid 2-acetyl-4-chloro-5-methyl-phenyl ester

: 143582-17-6
2-Benzoyl-5-chloro-6-methyl-benzofuran-3-one

Guidance literature:: With potassium hydroxide; [hydroxy(tosyloxy)iodo]benzene; Yield given. Multistep reaction; 1) dioxane, reflux, 2h, 2) KOH, rt to reflux, 0.5 h;
DOI:10.1055/s-1992-26179