1-(2-Phenylethyl)azepane

Base Information

Chemical Name:1-(2-Phenylethyl)azepane
CAS No.:65530-43-0
Molecular Formula:C14H21N
Molecular Weight:203.327
Hs Code.:
DSSTox Substance ID:DTXSID20558210
Nikkaji Number:J3.020.631B
Wikidata:Q82440418

Synonyms:1-(2-Phenylethyl)azepane;65530-43-0;SCHEMBL11922748;DTXSID20558210;AKOS017160936

Suppliers and Price of 1-(2-Phenylethyl)azepane

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-Phenylethyl)azepane

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:203.167399674
Heavy Atom Count:15
Complexity:153

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:C1CCCN(CC1)CCC2=CC=CC=C2

Technology Process of 1-(2-Phenylethyl)azepane

There total 5 articles about 1-(2-Phenylethyl)azepane 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: 85.0%

: 1072-21-5
hexanedial

: 64-04-0
phenethylamine

: 65530-43-0
N-(2-phenylethyl)perhydroazepine

Guidance literature:: With potassium hydroxide; tetracarbonylhydridoferrate; carbon monoxide; In ethanol; for 24h; Ambient temperature;

Reference yield: 63.0%

: 64-04-0
phenethylamine

: 110-83-8
cyclohexene

: 65530-43-0
N-(2-phenylethyl)perhydroazepine

Guidance literature:: cyclohexene; With oxygen; ozone; In methanol; dichloromethane; at -78 ℃;

phenethylamine; With sodium tris(acetoxy)borohydride; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1055/s-0030-1260244