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Norpropranolol, (+)-

Base Information
  • Chemical Name:Norpropranolol, (+)-
  • CAS No.:88547-39-1
  • Molecular Formula:C13H15 N O2
  • Molecular Weight:217.268
  • Hs Code.:
  • UNII:OTG4IE9L90
  • DSSTox Substance ID:DTXSID101255027
  • Nikkaji Number:J581.998I
  • Wikidata:Q27285837
Norpropranolol, (+)-

Synonyms:Norpropranolol, (+)-;UNII-OTG4IE9L90;OTG4IE9L90;88547-39-1;R(+)-1-Amino-3-(1-naphthyloxy)-2-propanol;(+)-norpropranolol;SCHEMBL9777869;DTXSID101255027;(R)-(+)-NDP;(R)-N-DESISOPROPYLPROPRANOLOL;(2R)-1-Amino-3-(1-naphthalenyloxy)-2-propanol;Q27285837;2-Propanol, 1-amino-3-(1-naphthalenyloxy)-, (2R)-;(2R)-(+)-1-(1-NAPHTHYLOXY)-3-AMINO-2-PROPANOL

Suppliers and Price of Norpropranolol, (+)-
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
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Chemical Property of Norpropranolol, (+)-
Chemical Property:
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:217.110278721
  • Heavy Atom Count:16
  • Complexity:210
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2OCC(CN)O
  • Isomeric SMILES:C1=CC=C2C(=C1)C=CC=C2OC[C@@H](CN)O
Technology Process of Norpropranolol, (+)-

There total 7 articles about Norpropranolol, (+)- 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:
Multi-step reaction with 5 steps
1: 60 percent / K2CO3 / dimethylformamide / 10 h / 100 °C
2: HCl-AcOH
3: TBAB
4: 79.4 percent / lipase (Pseudomonas sp.) / 24 h / 40 °C / pH 5
5: 81 percent / LAH
With hydrogenchloride; lithium aluminium tetrahydride; potassium carbonate; acetic acid; lipase (Pseudomonas sp.); tetrabutylammomium bromide; In N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(01)80880-7
Guidance literature:
Multi-step reaction with 4 steps
1: HCl-AcOH
2: TBAB
3: 79.4 percent / lipase (Pseudomonas sp.) / 24 h / 40 °C / pH 5
4: 81 percent / LAH
With hydrogenchloride; lithium aluminium tetrahydride; acetic acid; lipase (Pseudomonas sp.); tetrabutylammomium bromide;
DOI:10.1016/S0040-4039(01)80880-7
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