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(R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL

Base Information
  • Chemical Name:(R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL
  • CAS No.:1217757-71-5
  • Molecular Formula:C24H26N2O5
  • Molecular Weight:422.47
  • Hs Code.:
  • Mol file:1217757-71-5.mol
(R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL

Synonyms:(R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL;(R)-(+)-M4;(R)-(+)-BM 140830;(R)-3-[2-[[3-(9H-Carbazol-4-yloxy)-2-hydroxypropyl]amino]ethoxy]-4-methoxyphenol;(R)-5-Hydroxycarvedilol

Suppliers and Price of (R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL
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
  • TRC
  • (R)-(+)-5’-HydroxyphenylCarvedilol
  • 10mg
  • $ 1190.00
Total 8 raw suppliers
Chemical Property of (R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL
Chemical Property:
  • Melting Point:205-207°C 
  • Boiling Point:702.0±60.0 °C(Predicted) 
  • PKA:10.06±0.18(Predicted) 
  • PSA:95.97000 
  • Density:1.305±0.06 g/cm3(Predicted) 
  • LogP:3.83450 
  • Storage Temp.:-20°C Freezer 
Purity/Quality:

99% *data from raw suppliers

(R)-(+)-5’-HydroxyphenylCarvedilol *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses (R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL is an optically active metabolite of Carvedilol which is a multiple-action, neurohormonal antagonist that is used in the treatment of hypertension. An optically active metabolite of Carvedilol (C184625), a nonselective ?-adrenergic blocker with α1-blocking activity.
Technology Process of (R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL

There total 8 articles about (R)-(+)-5'-HYDROXYPHENYL-CARVEDILOL 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 lithium bromide; In isopropyl alcohol; for 12h; Reflux;
DOI:10.1016/j.bmcl.2015.11.008
Guidance literature:
Multi-step reaction with 2 steps
1.1: methylamine / methanol / 30 °C
1.2: 30 °C
2.1: triethylamine / isopropyl alcohol / 45 °C
With triethylamine; methylamine; In methanol; isopropyl alcohol;
DOI:10.1080/00397910903534072
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