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Thalifendine

Base Information Edit
  • Chemical Name:Thalifendine
  • CAS No.:18207-71-1
  • Molecular Formula:C19H16NO4+
  • Molecular Weight:322.34
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60171240
  • Wikidata:Q83041334
  • Metabolomics Workbench ID:122695
  • ChEMBL ID:CHEMBL1187148
  • Mol file:18207-71-1.mol
Thalifendine

Synonyms:thalifendine;thalifendine chloride

Suppliers and Price of Thalifendine
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
Total 36 raw suppliers
Chemical Property of Thalifendine Edit
Chemical Property:
  • PSA:52.85000 
  • LogP:3.07440 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:322.10793299
  • Heavy Atom Count:24
  • Complexity:474
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O
Technology Process of Thalifendine

There total 7 articles about Thalifendine 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: 85.0%

Guidance literature:
With methanesulfonyl chloride; triethylamine; In dichloromethane; at 20 ℃; for 6h;
Guidance literature:
With cytochrome CYP1A1; Reagent/catalyst; Kinetics; Enzymatic reaction;
DOI:10.1124/dmd.115.063966
Guidance literature:
With glucose-6-phosphate dehydrogenase; β-D-glucose 6-phosphate; NADP; magnesium chloride; cytochrome P450; In aq. phosphate buffer; dimethyl sulfoxide; at 37 ℃; for 0.5h; pH=7.4; Reagent/catalyst; Enzymatic reaction;
DOI:10.1124/dmd.115.063966
upstream raw materials:

berberine

berberine chloride

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