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Trimethoxy Dobutamine Hydrochloride

Base Information Edit
  • Chemical Name:Trimethoxy Dobutamine Hydrochloride
  • CAS No.:51062-14-7
  • Molecular Formula:C21H30ClNO3
  • Molecular Weight:379.93
  • Hs Code.:2922299000
  • European Community (EC) Number:610-606-2
  • DSSTox Substance ID:DTXSID10549839
  • Mol file:51062-14-7.mol
Trimethoxy Dobutamine Hydrochloride

Synonyms:Trimethoxy Dobutamine Hydrochloride;51062-14-7;N-[2-(3,4-dimethoxyphenyl)ethyl]-4-(4-methoxyphenyl)butan-2-amine;hydrochloride;4-[2-{[3-(4-Methoxy Phenyl)-1-Methylpropyl]amino]ethyl]-1,2-dimethoxybenzene hydrochloride;(2RS)-N-[2-(3,4-Dimethoxyphenyl)ethyl]-4-(4-methoxyphenyl)butan-2-amine Hydrochloride;SCHEMBL9817747;DTXSID10549839;4-(2-((3-(4-methoxyphenyl)-1-methylpropyl)amino)ethyl)-1,2-dimethoxybenzene hcl;N-[2-(3,4-Dimethoxyphenyl)ethyl]-4-(4-methoxyphenyl)butan-2-amine--hydrogen chloride (1/1)

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Chemical Property of Trimethoxy Dobutamine Hydrochloride Edit
Chemical Property:
  • PSA:39.72000 
  • LogP:5.05870 
  • Storage Temp.:Refrigerator 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:10
  • Exact Mass:379.1914215
  • Heavy Atom Count:26
  • Complexity:344
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CCC1=CC=C(C=C1)OC)NCCC2=CC(=C(C=C2)OC)OC.Cl
  • Uses Thrimethoxydobutamine is a trimethoxy precursor and impurity of Dobutamine (D494445).
Technology Process of Trimethoxy Dobutamine Hydrochloride

There total 6 articles about Trimethoxy Dobutamine 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:
4-(4-methoxyphenyl)-2-butanone; 2-(3,4-dimethoxyphenyl)-ethylamine; With 5%-palladium/activated carbon; ammonium formate; acetic acid; In dichloromethane; at 40 ℃; for 3h;
With hydrogenchloride; In water; for 1h; Reagent/catalyst;
Refernces Edit