2-Acetyl-4-methoxyphenyl benzoate

Base Information

Chemical Name:2-Acetyl-4-methoxyphenyl benzoate
CAS No.:127745-66-8
Molecular Formula:C16H14O4
Molecular Weight:270.285
Hs Code.:
DSSTox Substance ID:DTXSID50398126
Nikkaji Number:J502.022K
Wikidata:Q82199931
Mol file:127745-66-8.mol

Synonyms:127745-66-8;2-acetyl-4-methoxyphenyl benzoate;(2-acetyl-4-methoxyphenyl) benzoate;Ethanone, 1-[2-(benzoyloxy)-5-methoxyphenyl]-;F0347-3587;DTXSID50398126;AKOS024575957;Benzoic acid 2-acetyl-4-methoxyphenyl ester;SR-01000390686;SR-01000390686-1

Suppliers and Price of 2-Acetyl-4-methoxyphenyl benzoate

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 2 raw suppliers

Chemical Property of 2-Acetyl-4-methoxyphenyl benzoate

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:270.08920892
Heavy Atom Count:20
Complexity:346

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2-Acetyl-4-methoxyphenyl benzoate

There total 2 articles about 2-Acetyl-4-methoxyphenyl benzoate 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: 63.0%

: 705-15-7
1-(2-hydroxy-5-methoxyphenyl)ethan-1-one

: 70-11-1
α-bromoacetophenone

: 127745-66-8
2-(benzyloxy)-5-(methoxy)acetophenone

Guidance literature:: With copper(II) acetate monohydrate; In tert-Amyl alcohol; at 100 ℃; for 10h;
DOI:10.1039/c7cc05383e

Reference yield:

: 490-78-8
2,5-Dihydroxyacetophenone

: 127745-66-8
2-(benzyloxy)-5-(methoxy)acetophenone

Guidance literature:: Multi-step reaction with 2 steps

1: 62.3 percent / aq. K₂CO₃ / acetone / 3 h / Heating

2: 70.5 percent / pyridine / 0.5 h / 50 °C

With pyridine; potassium carbonate; In acetone;
DOI:10.1002/jccs.200400203