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Technology Process of (R)-Bopindolol

(R)-Bopindolol

Base Information
  • Chemical Name:(R)-Bopindolol
  • CAS No.:62697-43-2
  • Molecular Formula:C23H28N2O3
  • Molecular Weight:380.48000
  • Hs Code.:
  • UNII:86A9F5821S
  • Nikkaji Number:J238.755G
  • Mol file:62697-43-2.mol
(R)-Bopindolol

Synonyms:(R)-Bopindolol;Bopindolol, (R)-;62697-43-2;86A9F5821S;UNII-86A9F5821S;2-Propanol, 1-((1,1-dimethylethyl)amino)-3-((2-methyl-1H-indol-4-yl)oxy)-, 2-benzoate, (2R)-;2-Propanol, 1-((1,1-dimethylethyl)amino)-3-((2-methyl-1H-indol-4-yl)oxy)-, benzoate (ester), (2R)-;2-Propanol, 1-((1,1-dimethylethyl)amino)-3-((2-methyl-1H-indol-4-yl)oxy)-, benzoate (ester), (R)-;SCHEMBL49501;CHEBI:143780;(R)-1-(tert-Butylamino)-3-[(2-methyl-1H-indol-4-yl)oxy]-2-benzoyloxypropane;PD132900;(2R)-1-(tert-butylamino)-3-[(2-methyl-1H-indol-4-yl)oxy]propan-2-yl benzoate;[(2R)-1-(tert-butylamino)-3-[(2-methyl-1H-indol-4-yl)oxy]propan-2-yl] benzoate

Suppliers and Price of (R)-Bopindolol
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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Total 0 raw suppliers
Chemical Property of (R)-Bopindolol
Chemical Property:
  • PSA：63.35000 
  • LogP:4.85970 
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:9
  • Exact Mass:380.20999276
  • Heavy Atom Count:28
  • Complexity:499
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1=CC2=C(N1)C=CC=C2OCC(CNC(C)(C)C)OC(=O)C3=CC=CC=C3
  • Isomeric SMILES:CC1=CC2=C(N1)C=CC=C2OC[C@@H](CNC(C)(C)C)OC(=O)C3=CC=CC=C3
Technology Process of (R)-Bopindolol

There total 1 articles about (R)-Bopindolol 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:

Reference yield:

bopindolol
69010-88-4

bopindolol

(S)-bopindolol
62697-41-0,69010-88-4

(S)-bopindolol

C<sub>23</sub>H<sub>28</sub>N<sub>2</sub>O<sub>3</sub>
62697-43-2,69010-88-4

C23H28N2O3

Guidance literature:
With AmyCoat (150x46 mm, 3 μm size silica particle); In ethanol; n-heptane; diethylamine; at 27 ℃; Resolution of racemate;
DOI:10.1002/chir.20697
upstream raw materials:

bopindolol

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