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Apilimod mesylate

Base Information
  • Chemical Name:Apilimod mesylate
  • CAS No.:870087-36-8
  • Molecular Formula:CH4O3S*C23H26N6O2
  • Molecular Weight:514.605
  • Hs Code.:
  • European Community (EC) Number:810-042-9
  • UNII:5G3P5OK11S
  • NCI Thesaurus Code:C90809
  • Mol file:870087-36-8.mol
Apilimod mesylate

Synonyms:apilimod;apilimod bis-mesylate;apilimod bismesylate;apilimod dimesylate;apilimod mesilate;apilimod mesylate;STA 5326;STA 5326 mesilate;STA 5326 mesylate;STA-5326;STA-5326 mesilate;STA-5326 mesylate;STA5326

Suppliers and Price of Apilimod mesylate
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
  • Tocris
  • Apilimoddimesylate ≥98%(HPLC)
  • 5
  • $ 139.00
  • DC Chemicals
  • Apilimodmesylate >98%
  • 250 mg
  • $ 1100.00
  • DC Chemicals
  • Apilimodmesylate >98%
  • 100 mg
  • $ 650.00
  • ChemScene
  • Apilimod(mesylate) 99.40%
  • 50mg
  • $ 120.00
  • ChemScene
  • Apilimod(mesylate) 99.40%
  • 10mg
  • $ 80.00
  • ChemScene
  • Apilimod(mesylate) 99.40%
  • 5mg
  • $ 50.00
  • ChemScene
  • Apilimod(mesylate) 99.40%
  • 100mg
  • $ 520.00
  • Biosynth Carbosynth
  • Apilimod mesylate NEW
  • 100 mg
  • $ 500.00
  • Biosynth Carbosynth
  • Apilimod mesylate NEW
  • 50 mg
  • $ 375.00
  • Biosynth Carbosynth
  • Apilimod mesylate NEW
  • 25 mg
  • $ 250.00
Total 22 raw suppliers
Chemical Property of Apilimod mesylate
Chemical Property:
  • PSA:210.26000 
  • LogP:4.39170 
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:14
  • Rotatable Bond Count:8
  • Exact Mass:610.18795441
  • Heavy Atom Count:41
  • Complexity:637
Purity/Quality:

99%, *data from raw suppliers

Apilimoddimesylate ≥98%(HPLC) *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1=CC(=CC=C1)C=NNC2=CC(=NC(=N2)OCCC3=CC=CC=N3)N4CCOCC4.CS(=O)(=O)O.CS(=O)(=O)O
  • Isomeric SMILES:CC1=CC(=CC=C1)/C=N/NC2=CC(=NC(=N2)OCCC3=CC=CC=N3)N4CCOCC4.CS(=O)(=O)O.CS(=O)(=O)O
  • Recent ClinicalTrials:A Study of LAM-002A for the Prevention of Progression of COVID-19
  • Recent EU Clinical Trials:A Randomized, Double-blind, Placebo-controlled Clinical Study of the Oral IL-12/23 Inhibitor, STA-5326 mesylate, for the Induction of Clinical Response in Patients with Crohn’s Disease
Technology Process of Apilimod mesylate

There total 2 articles about Apilimod mesylate 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 ethanol; toluene; at 20 ℃; Product distribution / selectivity;
upstream raw materials:

methanesulfonic acid

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