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Tedatioxetine

Base Information Edit
  • Chemical Name:Tedatioxetine
  • CAS No.:508233-95-2
  • Molecular Formula:C18H21NS
  • Molecular Weight:283.437
  • Hs Code.:
  • UNII:5H681S8O3S
  • DSSTox Substance ID:DTXSID801029350
  • Wikipedia:Tedatioxetine
  • Wikidata:Q7693930
  • NCI Thesaurus Code:C152535
  • Metabolomics Workbench ID:153591
  • ChEMBL ID:CHEMBL2104986
  • Mol file:508233-95-2.mol
Tedatioxetine

Synonyms:Lu AA24530;Tedatioxetine

Suppliers and Price of Tedatioxetine
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 3 raw suppliers
Chemical Property of Tedatioxetine Edit
Chemical Property:
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:283.13947085
  • Heavy Atom Count:20
  • Complexity:279
Purity/Quality:

98% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=C(C=C1)SC2=CC=CC=C2C3CCNCC3
  • Recent ClinicalTrials:Dose-finding Study With Lu AA24530 in Major Depressive Disorder
  • Recent EU Clinical Trials:Randomised, double-blind, parallel-group, placebo-controlled, duloxetine-referenced, dose-finding study of Lu AA24530 in Major Depressive Disorder
Technology Process of Tedatioxetine

There total 6 articles about Tedatioxetine 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 sodium hydroxide; In water; ethyl acetate; for 0.25h; pH=13 - 14;
Guidance literature:
Multi-step reaction with 2 steps
1: hydrogen bromide; acetic acid / 18 h / 80 °C
2: sodium hydroxide / ethyl acetate / 0.25 h / pH 13 - 14
With hydrogen bromide; acetic acid; sodium hydroxide; In ethyl acetate;
Guidance literature:
Multi-step reaction with 4 steps
1.1: potassium tert-butylate / 1-methyl-pyrrolidin-2-one / 120 °C / Inert atmosphere
2.1: n-butyllithium / n-heptane; hexane / 1.17 h / 20 °C / Inert atmosphere
2.2: -40 °C
3.1: hydrogen bromide; acetic acid / 18 h / 80 °C
4.1: sodium hydroxide / ethyl acetate / 0.25 h / pH 13 - 14
With n-butyllithium; potassium tert-butylate; hydrogen bromide; acetic acid; sodium hydroxide; In 1-methyl-pyrrolidin-2-one; hexane; n-heptane; ethyl acetate;
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