N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide

Base Information

Chemical Name:N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide
CAS No.:88951-63-7
Molecular Formula:C15H12ClNO3
Molecular Weight:289.718
Hs Code.:
DSSTox Substance ID:DTXSID30368322
Wikidata:Q82154766

Synonyms:N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide;88951-63-7;SCHEMBL2557846;DTXSID30368322;BBL024283;MFCD03961634;STK200431;AKOS000194912;VS-07777;CS-0257836;EN300-68237;N-(4-Chloro-phenyl)-2-(4-formyl-phenoxy)-acetamide;Z19658474

Suppliers and Price of N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide

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 6 raw suppliers

Chemical Property of N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:289.0505709
Heavy Atom Count:20
Complexity:321

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C=O)OCC(=O)NC2=CC=C(C=C2)Cl

Technology Process of N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide

There total 5 articles about N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide 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: 99.0%

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 3289-75-6
2-chloro-N-(4-chlorophenyl)acetamide

: 88951-63-7
p-formylphenyl p-chlorophenylcarbamoylmethyl ether

Guidance literature:: With potassium carbonate; potassium iodide; In acetone; for 24h; Reflux;
DOI:10.1021/jm1011534

Reference yield: 67.0%

: 22666-84-8
4-hydroxybenzaldehyde sodium salt

: 3289-75-6
2-chloro-N-(4-chlorophenyl)acetamide

: 88951-63-7
p-formylphenyl p-chlorophenylcarbamoylmethyl ether

Guidance literature:: In N,N-dimethyl-formamide; for 4h; Heating;

Reference yield:

: 106-47-8
4-chloro-aniline

: 88951-63-7
p-formylphenyl p-chlorophenylcarbamoylmethyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 0 - 25 °C

2: potassium carbonate; potassium iodide / acetone / 24 h / Reflux

With potassium carbonate; triethylamine; potassium iodide; In dichloromethane; acetone;
DOI:10.1021/jm1011534