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(R)-Monodes(isopropyl)disopyramide

Base Information
  • Chemical Name:(R)-Monodes(isopropyl)disopyramide
  • CAS No.:77494-40-7
  • Molecular Formula:C18H23N3O
  • Molecular Weight:297.4
  • Hs Code.:
  • UNII:9VSB59XC1V
  • ChEMBL ID:CHEMBL2111241
  • Nikkaji Number:J444.340C
  • Wikidata:Q27273288
(R)-Monodes(isopropyl)disopyramide

Synonyms:(R)-Monodes(isopropyl)disopyramide;UNII-9VSB59XC1V;(-)-Mono-N-desisopropyldisopyramide;9VSB59XC1V;(R)-(-)-Mono-N-des(isopropyl)disopyramide;77494-40-7;2-Pyridineacetamide, alpha-(2-((1-methylethyl)amino)ethyl)-alpha-phenyl-, (alphaR)-;CHEMBL2111241;Q27273288;2-PYRIDINEACETAMIDE, .ALPHA.-(2-((1-METHYLETHYL)AMINO)ETHYL)-.ALPHA.-PHENYL-, (.ALPHA.R)-

Suppliers and Price of (R)-Monodes(isopropyl)disopyramide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of (R)-Monodes(isopropyl)disopyramide
Chemical Property:
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:7
  • Exact Mass:297.184112366
  • Heavy Atom Count:22
  • Complexity:352
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)NCCC(C1=CC=CC=C1)(C2=CC=CC=N2)C(=O)N
  • Isomeric SMILES:CC(C)NCC[C@@](C1=CC=CC=C1)(C2=CC=CC=N2)C(=O)N
Technology Process of (R)-Monodes(isopropyl)disopyramide

There total 4 articles about (R)-Monodes(isopropyl)disopyramide 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 potassium carbonate; zinc; In ethanol; for 0.333333h; Yield given; Ambient temperature;
DOI:10.1021/jm00137a024
Guidance literature:
Multi-step reaction with 4 steps
2: m-chloroperoxybenzoic acid / CH2Cl2 / 0.5 h / Ambient temperature
3: benzene / 0.17 h / Heating
4: Zn, K2CO3 / aq. ethanol / 0.33 h / Ambient temperature
With potassium carbonate; 3-chloro-benzenecarboperoxoic acid; zinc; In ethanol; dichloromethane; benzene;
DOI:10.1021/jm00137a024
Guidance literature:
Multi-step reaction with 3 steps
1: m-chloroperoxybenzoic acid / CH2Cl2 / 0.5 h / Ambient temperature
2: benzene / 0.17 h / Heating
3: Zn, K2CO3 / aq. ethanol / 0.33 h / Ambient temperature
With potassium carbonate; 3-chloro-benzenecarboperoxoic acid; zinc; In ethanol; dichloromethane; benzene;
DOI:10.1021/jm00137a024
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