Benzoic acid, 4-methoxy-, 2-acetyl-4-bromophenyl ester

Base Information

Chemical Name:Benzoic acid, 4-methoxy-, 2-acetyl-4-bromophenyl ester
CAS No.:88952-06-1
Molecular Formula:C16H13BrO4
Molecular Weight:349.181
Hs Code.:
DSSTox Substance ID:DTXSID00470441
Wikidata:Q82298534

Synonyms:Benzoic acid, 4-methoxy-, 2-acetyl-4-bromophenyl ester;88952-06-1;SCHEMBL4993947;DTXSID00470441;GWFRPCKHLQSHDL-UHFFFAOYSA-N;4-methoxybenzoic acid 2-acetyl-4-bromophenyl ester

Suppliers and Price of Benzoic acid, 4-methoxy-, 2-acetyl-4-bromophenyl ester

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 Benzoic acid, 4-methoxy-, 2-acetyl-4-bromophenyl ester

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:347.99972
Heavy Atom Count:21
Complexity:377

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)Br)OC(=O)C2=CC=C(C=C2)OC

Technology Process of Benzoic acid, 4-methoxy-, 2-acetyl-4-bromophenyl ester

There total 1 articles about Benzoic acid, 4-methoxy-, 2-acetyl-4-bromophenyl 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: 96.5%

: 1450-75-5
5-Bromo-2-hydroxyacetophenone

: 100-07-2
4-methoxy-benzoyl chloride

: 88952-06-1
4-methoxybenzoic acid 2-acetyl-4-bromophenyl ester

Guidance literature:: With pyridine; for 0.583333h;
DOI:10.1021/jm050635e

Reference yield: 85.2%

: 88952-06-1
4-methoxybenzoic acid 2-acetyl-4-bromophenyl ester

: 88952-44-7
1-(5-bromo-2-hydroxyphenyl)-3-(4-methoxyphenyl)propane-1,3-dione

Guidance literature:: With pyridine; potassium hydroxide; at 50 ℃; for 0.25h;
DOI:10.1021/jm050635e

Reference yield:

: 88952-06-1
4-methoxybenzoic acid 2-acetyl-4-bromophenyl ester

: 288401-01-4
6-bromo-4'-hydroxyflavone

Guidance literature:: Multi-step reaction with 3 steps

1: 85.2 percent / KOH; pyridine / 0.25 h / 50 °C

2: 79.4 percent / H₂SO₄; AcOH / 1 h / Heating

3: 13.1 percent / BBr₃ / CH₂Cl₂ / 6 h / 20 °C

With pyridine; potassium hydroxide; sulfuric acid; boron tribromide; acetic acid; In dichloromethane;
DOI:10.1021/jm050635e