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Iprindole

Base Information Edit
  • Chemical Name:Iprindole
  • CAS No.:5560-72-5
  • Molecular Formula:C19H28 N2
  • Molecular Weight:284.445
  • Hs Code.:
  • European Community (EC) Number:226-933-5
  • NSC Number:169449
  • UNII:69U0IKR8FP
  • DSSTox Substance ID:DTXSID80204145
  • Nikkaji Number:J9.552D
  • Wikipedia:Iprindole
  • Wikidata:Q904673
  • NCI Thesaurus Code:C166921
  • Metabolomics Workbench ID:154299
  • ChEMBL ID:CHEMBL126224
  • Mol file:5560-72-5.mol
Iprindole

Synonyms:Iprindole

Suppliers and Price of Iprindole
Supply Marketing:Edit
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
  • Iprindole
  • 50mg
  • $ 495.00
  • ChemScene
  • Iprindole 98.02%
  • 50mg
  • $ 420.00
  • ChemScene
  • Iprindole 98.02%
  • 25mg
  • $ 250.00
  • ChemScene
  • Iprindole 98.02%
  • 10mg
  • $ 120.00
  • ChemScene
  • Iprindole 98.02%
  • 100mg
  • $ 700.00
  • American Custom Chemicals Corporation
  • IPRINDOLE 95.00%
  • 5MG
  • $ 502.22
Total 5 raw suppliers
Chemical Property of Iprindole Edit
Chemical Property:
  • Vapor Pressure:8.78E-08mmHg at 25°C 
  • Refractive Index:1.8676 (estimate) 
  • Boiling Point:435.4°Cat760mmHg 
  • PKA:pKa 8.2 (Uncertain) 
  • Flash Point:217.1°C 
  • PSA:8.17000 
  • Density:1.04g/cm3 
  • LogP:4.25200 
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:4
  • Exact Mass:284.225248902
  • Heavy Atom Count:21
  • Complexity:315
Purity/Quality:

99% *data from raw suppliers

Iprindole *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN(C)CCCN1C2=C(CCCCCC2)C3=CC=CC=C31
  • Uses Antidepressant. Chronic administration of atypical antidepressant, Iprindole, was effective in reversing learned helplessness.
Technology Process of Iprindole

There total 7 articles about Iprindole 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:
cyclooctyl bromide; With chloro-trimethyl-silane; magnesium; ethylene dibromide; lithium chloride; zinc dibromide; In tetrahydrofuran; at 25 ℃; for 2h; Inert atmosphere;
benzenediazonium tetrafluoroborate; In tetrahydrofuran; at -60 - 25 ℃; Inert atmosphere;
3-(Dimethylamino)propyl chloride; Further stages;
DOI:10.1002/anie.201005319
Guidance literature:
6,7,8,9,10,11-Hexahydro-5H-cycloocta[b]indole; With potassium tert-butylate; tetra-(n-butyl)ammonium iodide; In N,N-dimethyl-formamide; at 20 ℃; for 2h; Inert atmosphere;
3-(Dimethylamino)propyl chloride; In N,N-dimethyl-formamide; at 60 - 120 ℃; for 5.5h; Inert atmosphere;
DOI:10.1002/anie.201202971
Guidance literature:
Multi-step reaction with 4 steps
1.1: indium; trifuran-2-yl-phosphane; palladium diacetate; lithium iodide / N,N-dimethyl-formamide / 5 h / 110 °C / Inert atmosphere; Molecular sieve
2.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 66 h / 20 °C / 7600.51 Torr / Autoclave
3.1: ethanol; potassium hydroxide / 14 h / 80 °C / Inert atmosphere
4.1: potassium tert-butylate; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 2 h / 20 °C / Inert atmosphere
4.2: 5.5 h / 60 - 120 °C / Inert atmosphere
With indium; trifuran-2-yl-phosphane; ethanol; palladium 10% on activated carbon; potassium tert-butylate; hydrogen; palladium diacetate; tetra-(n-butyl)ammonium iodide; potassium hydroxide; lithium iodide; In ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1002/anie.201202971
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