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Edan hydrochloride

Base Information
  • Chemical Name:Edan hydrochloride
  • CAS No.:3861-78-7
  • Molecular Formula:C15H21NO4*ClH
  • Molecular Weight:315.797
  • Hs Code.:
  • UNII:J0TQX5LV1L
  • Wikidata:Q27280999
  • Mol file:3861-78-7.mol
Edan hydrochloride

Synonyms:diethylaminoethyl acetylsalicylate;Edan;Edan hydrochloride

Suppliers and Price of Edan hydrochloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 1 raw suppliers
Chemical Property of Edan hydrochloride
Chemical Property:
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:9
  • Exact Mass:315.1237359
  • Heavy Atom Count:21
  • Complexity:315
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCN(CC)CCOC(=O)C1=CC=CC=C1OC(=O)C.Cl
  • Recent ClinicalTrials:Evaluate the Efficacy and Safety of TF0023 in Treatments for COVID-19 in Hospitalized Adults
  • Recent EU Clinical Trials:A Phase 2, Multicenter, Randomized, Double-blind (Within Dose), Placebo-controlled, Parallel-group, and Dose-range-finding Study to Evaluate the Efficacy and Safety of TF0023 Versus Placebo in Treatments for COVID-19 in Hospitalized Adults
Technology Process of Edan hydrochloride

There total 2 articles about Edan hydrochloride 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:
aspirin; With thionyl chloride; In ethyl acetate; for 3h; Reflux;
2-(Diethylamino)ethanol; With sodium hydrogencarbonate; In ethyl acetate; at 5 - 20 ℃;
With hydrogenchloride;
Guidance literature:
Multi-step reaction with 2 steps
1: thionyl chloride / ethyl acetate / 3 h / Reflux
2: sodium hydrogencarbonate / ethyl acetate / 5 - 20 °C
With thionyl chloride; sodium hydrogencarbonate; In ethyl acetate;
Guidance literature:
With hydrogenchloride; In water; acetonitrile; at 20 ℃; for 48h;
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