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Mepixanox

Base Information
  • Chemical Name:Mepixanox
  • CAS No.:17854-59-0
  • Molecular Formula:C20H21NO3
  • Molecular Weight:323.392
  • Hs Code.:2934999090
  • European Community (EC) Number:241-810-6
  • UNII:7419T4YQQW
  • DSSTox Substance ID:DTXSID90170504
  • Nikkaji Number:J107.253F
  • Wikipedia:Mepixanox
  • Wikidata:Q6817820
  • NCI Thesaurus Code:C66094
  • Metabolomics Workbench ID:154373
  • ChEMBL ID:CHEMBL2104462
  • Mol file:17854-59-0.mol
Mepixanox

Synonyms:3-methoxy-4-(piperidinomethyl)xanthone;mepixanox;pimexone;pimexone hydrochloride

Suppliers and Price of Mepixanox
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 6 raw suppliers
Chemical Property of Mepixanox
Chemical Property:
  • Vapor Pressure:1.13E-09mmHg at 25°C 
  • Melting Point:159-160° 
  • Boiling Point:488°Cat760mmHg 
  • PKA:8.33±0.10(Predicted) 
  • Flash Point:249°C 
  • PSA:42.68000 
  • Density:1.224g/cm3 
  • LogP:3.87860 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:323.15214353
  • Heavy Atom Count:24
  • Complexity:448
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3O2)CN4CCCCC4
  • Description Mepixanox is a respiratory stimulant useful in the treatment of chronic pneumopathy and other cardiorespiratory insufficiencies, including those induced by general anesthesia.
Technology Process of Mepixanox

There total 6 articles about Mepixanox 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:
In N,N-dimethyl-formamide; for 2h; Ambient temperature;

Reference yield:

Guidance literature:
Aus entspr. 4-Brommethylverb. m. Piperidin;
Guidance literature:
Multi-step reaction with 4 steps
1: 82.7 percent / copper-bronze, copper(I) iodide, K2CO3 / dimethylformamide / 4 h / 140 °C
2: 101 g / conc. H2SO4 / 1 h / 50 °C
3: 9 g / AcOH, aq. HCl / 2 h / 60 °C
4: 89 percent / dimethylformamide / 2 h / Ambient temperature
With hydrogenchloride; copper(l) iodide; sulfuric acid; copper; potassium carbonate; acetic acid; In N,N-dimethyl-formamide;
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