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3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine

Base Information
  • Chemical Name:3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine
  • CAS No.:73823-53-7
  • Molecular Formula:C16H24N2O2
  • Molecular Weight:276.379
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50994889
  • Nikkaji Number:J87.497C
3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine

Synonyms:BRN 5272684;2-Propanol, 1-phenoxy-3-(3-quinuclidinylamino)-;3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine;73823-53-7;SCHEMBL20553036;DTXSID50994889;LS-122626;1-Phenoxy-3-(3-quinuclidinylamino)-2-propanol;1-[(1-Azabicyclo[2.2.2]octan-3-yl)amino]-3-phenoxypropan-2-ol

Suppliers and Price of 3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine
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 3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine
Chemical Property:
  • Vapor Pressure:8.53E-09mmHg at 25°C 
  • Boiling Point:447.6°Cat760mmHg 
  • Flash Point:224.5°C 
  • Density:1.17g/cm3 
  • XLogP3:1.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:276.183778013
  • Heavy Atom Count:20
  • Complexity:286
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CN2CCC1C(C2)NCC(COC3=CC=CC=C3)O
Technology Process of 3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine

There total 3 articles about 3-(beta-Hydroxy-gamma-phenoxypropylamino)quinuclidine 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 sodium tetrahydroborate; In ethanol; for 20h; Ambient temperature;
DOI:10.1007/BF00765604
Guidance literature:
Multi-step reaction with 2 steps
1: 55 percent / p-toluenesulfonic acid / toluene / 10 h / Heating
2: 69 percent / sodium borohydride / ethanol / 20 h / Ambient temperature
With sodium tetrahydroborate; toluene-4-sulfonic acid; In ethanol; toluene;
DOI:10.1007/BF00765604
Guidance literature:
Multi-step reaction with 2 steps
1: 55 percent / p-toluenesulfonic acid / toluene / 10 h / Heating
2: 69 percent / sodium borohydride / ethanol / 20 h / Ambient temperature
With sodium tetrahydroborate; toluene-4-sulfonic acid; In ethanol; toluene;
DOI:10.1007/BF00765604
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