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Milameline hydrochloride

Base Information
  • Chemical Name:Milameline hydrochloride
  • CAS No.:139886-04-7
  • Deprecated CAS:147414-43-5
  • Molecular Formula:C8H14N2O*ClH
  • Molecular Weight:190.673
  • Hs Code.:
  • UNII:W867E71LPD
  • NCI Thesaurus Code:C91040
  • ChEMBL ID:CHEMBL2106918
  • Mol file:139886-04-7.mol
Milameline hydrochloride

Synonyms:1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxaldehyde O-methyloxime monohydrochloride;CI 979;CI 979, (E)-isomer HCl;CI-979;CI979;milameline

Suppliers and Price of Milameline hydrochloride
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
  • MilamelineHydrochloride
  • 5mg
  • $ 305.00
  • ApexBio Technology
  • Milamelinehydrochloride
  • 50mg
  • $ 1032.00
  • ApexBio Technology
  • Milamelinehydrochloride
  • 10mg
  • $ 245.00
Total 2 raw suppliers
Chemical Property of Milameline hydrochloride
Chemical Property:
  • Vapor Pressure:0.109mmHg at 25°C 
  • Boiling Point:221.1°Cat760mmHg 
  • Flash Point:87.5°C 
  • PSA:24.83000 
  • Density:g/cm3 
  • LogP:1.62040 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:190.0872908
  • Heavy Atom Count:12
  • Complexity:175
Purity/Quality:

98% *data from raw suppliers

MilamelineHydrochloride *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1CCC=C(C1)C=NOC.Cl
  • Isomeric SMILES:CN1CCC=C(C1)/C=N/OC.Cl
  • Uses Antidementia (partial muscarinic agonist. Milameline Hydrochloride is a muscarinic cholinergic agonist on acetylcholine and dopamine receptors providing cognition-activating properties.
Technology Process of Milameline hydrochloride

There total 1 articles about Milameline 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:
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