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Hydrodolasetron

Base Information
  • Chemical Name:Hydrodolasetron
  • CAS No.:127951-99-9
  • Molecular Formula:C19H22N2O3
  • Molecular Weight:326.395
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90926043
  • Nikkaji Number:J1.037.899K
  • Pharos Ligand ID:UHRBN2CWXJF6
  • ChEMBL ID:CHEMBL498572
  • Mol file:127951-99-9.mol
Hydrodolasetron

Synonyms:1-H-indole-3-carboxylic acid, trans-octahydro-3-hydroxy-2,6-methano-2H-quinolizin-8-yl ester;hydrodolasetron;MDL 74156;MDL-74156

Suppliers and Price of Hydrodolasetron
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
  • TRC
  • Hydrodolasetron
  • 5mg
  • $ 150.00
  • Medical Isotopes, Inc.
  • Hydrodolasetron
  • 50 mg
  • $ 2200.00
  • American Custom Chemicals Corporation
  • HYDRODOLASETRON (RACEMIC) 95.00%
  • 5MG
  • $ 495.46
Total 17 raw suppliers
Chemical Property of Hydrodolasetron
Chemical Property:
  • Vapor Pressure:2.9E-12mmHg at 25°C 
  • Boiling Point:534.7°Cat760mmHg 
  • PKA:14.59±0.40(Predicted) 
  • Flash Point:277.2°C 
  • PSA:65.56000 
  • Density:1.37g/cm3 
  • LogP:2.24870 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:326.16304257
  • Heavy Atom Count:24
  • Complexity:497
Purity/Quality:

99% *data from raw suppliers

Hydrodolasetron *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1C2CC3CC(CC1N3CC2O)OC(=O)C4=CNC5=CC=CC=C54
  • Uses Hydrodolasetron, is the reduced form of Dolasetron (D528500), a specific serotonin (5HT3) receptor antagonist. Antiemetic.
Technology Process of Hydrodolasetron

There total 1 articles about Hydrodolasetron 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:
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