[2-(2-Aminoethoxy)-5-chlorophenyl](phenyl)methanone

Base Information

Chemical Name:[2-(2-Aminoethoxy)-5-chlorophenyl](phenyl)methanone
CAS No.:69149-42-4
Molecular Formula:C₁₅H₁₄ClNO₂
Molecular Weight:275.735
Hs Code.:
DSSTox Substance ID:DTXSID80529441
Wikidata:Q82399861

Synonyms:69149-42-4;[2-(2-Aminoethoxy)-5-chlorophenyl](phenyl)methanone;SCHEMBL11640622;DTXSID80529441

Suppliers and Price of [2-(2-Aminoethoxy)-5-chlorophenyl](phenyl)methanone

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 [2-(2-Aminoethoxy)-5-chlorophenyl](phenyl)methanone

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:275.0713064
Heavy Atom Count:19
Complexity:292

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:C1=CC=C(C=C1)C(=O)C2=C(C=CC(=C2)Cl)OCCN

Technology Process of [2-(2-Aminoethoxy)-5-chlorophenyl](phenyl)methanone

There total 5 articles about [2-(2-Aminoethoxy)-5-chlorophenyl](phenyl)methanone 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: 64.0%

: 69149-42-4
2-(2-aminoethoxy)-5-chlorobenzophenone

Guidance literature:

Reference yield:

: 89718-93-4
2-[4-Chloro-2-(2-phenyl-[1,3]dioxolan-2-yl)-phenoxy]-ethylamine

: 69149-42-4
2-(2-aminoethoxy)-5-chlorobenzophenone

: 29165-23-9
7-chloro-5-phenyl-2,3-dihydrobenzo[f][1,4]oxazepine

Guidance literature:: With hydrogenchloride; In methanol; at 50 - 55 ℃; for 3h;

Reference yield:

: 85-19-8
(5-chloro-2-hydroxyphenyl)phenylmethanone

: 69149-42-4
2-(2-aminoethoxy)-5-chlorobenzophenone

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) potassium iodide, 2.) potassium carbonate / 1.) butanone, 18 h, 2.) butanone, reflux, 1.5 h

2: 90 percent / p-toluenesulfonic acid / benzene / 7.5 h / Heating

3: lithium tetrahydroaluminate / diethyl ether / 2 h / Heating

4: methanolic hydrochloric acid / 3 h / 50 - 55 °C

With hydrogenchloride; lithium aluminium tetrahydride; potassium carbonate; toluene-4-sulfonic acid; potassium iodide; In diethyl ether; benzene;