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Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride

Base Information
  • Chemical Name:Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride
  • CAS No.:5221-18-1
  • Molecular Formula:C14H15NO2.ClH
  • Molecular Weight:265.74
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10459525
Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride

Synonyms:5221-18-1;Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride;THYRONAMINE HYDROCHLORIDE;DTXSID10459525

Suppliers and Price of Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride
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 4 raw suppliers
Chemical Property of Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride
Chemical Property:
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:265.0869564
  • Heavy Atom Count:18
  • Complexity:206
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC=C1CCN)OC2=CC=C(C=C2)O.Cl
Technology Process of Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride

There total 7 articles about Phenol, 4-[4-(2-aminoethyl)phenoxy]-, hydrochloride 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:
Guidance literature:
With hydrogenchloride; In ethyl acetate; at 20 ℃;
DOI:10.1021/jm0505718
Guidance literature:
Multi-step reaction with 4 steps
1: 91 percent / aq. NaHCO3 / tetrahydrofuran / 24 h
2: 40 percent / Cu(OAc)2; Et3N; pyridine / 4 Angstroem molecular sieves / CH2Cl2 / 20 °C
3: 86 percent / TBAF / tetrahydrofuran / 0 °C
4: 100 percent / HCl / ethyl acetate / 20 °C
With pyridine; hydrogenchloride; copper diacetate; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; triethylamine; 4 A molecular sieve; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1021/jm0505718
Guidance literature:
Multi-step reaction with 5 steps
1.1: 82 percent / imidazole / CH2Cl2 / 12.5 h / 0 - 20 °C
2.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C
2.2: triisopropyl borate / tetrahydrofuran; hexane / 5 h / -78 - 20 °C
2.3: 68 percent / aq. HCl / tetrahydrofuran; hexane / 0.5 h / 0 °C
3.1: 40 percent / Cu(OAc)2; Et3N; pyridine / 4 Angstroem molecular sieves / CH2Cl2 / 20 °C
4.1: 86 percent / TBAF / tetrahydrofuran / 0 °C
5.1: 100 percent / HCl / ethyl acetate / 20 °C
With pyridine; 1H-imidazole; hydrogenchloride; n-butyllithium; copper diacetate; tetrabutyl ammonium fluoride; triethylamine; 4 A molecular sieve; In tetrahydrofuran; hexane; dichloromethane; ethyl acetate;
DOI:10.1021/jm0505718
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