Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Oxotremorine

Base Information Edit
  • Chemical Name:Oxotremorine
  • CAS No.:70-22-4
  • Molecular Formula:C12H18N2O
  • Molecular Weight:206.288
  • Hs Code.:
  • European Community (EC) Number:200-728-0
  • NSC Number:330497
  • UNII:5RY0UWH1JL
  • DSSTox Substance ID:DTXSID10220252
  • Nikkaji Number:J1.421D
  • Wikipedia:Oxotremorine
  • Wikidata:Q676896
  • NCI Thesaurus Code:C67048
  • Pharos Ligand ID:NUX1N7J2S33B
  • Metabolomics Workbench ID:67481
  • ChEMBL ID:CHEMBL7634
  • Mol file:70-22-4.mol
Oxotremorine

Synonyms:Oxotremorine;Oxytremorine

Suppliers and Price of Oxotremorine
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
  • American Custom Chemicals Corporation
  • 1-[4-(1-PYRROLIDINYL)-2-BUTYNYL]-2-PYRROLIDINONE 95.00%
  • 5MG
  • $ 496.89
  • AHH
  • Oxotremorine 97%
  • 25g
  • $ 330.00
Total 14 raw suppliers
Chemical Property of Oxotremorine Edit
Chemical Property:
  • Vapor Pressure:8.7E-06mmHg at 25°C 
  • Refractive Index:n20/D 1.517(lit.) 
  • Boiling Point:124 °C0.1 mm Hg(lit.)  
  • Flash Point:113 °C 
  • PSA:23.55000 
  • Density:1 g/mL at 25 °C(lit.)  
  • LogP:0.58380 
  • Storage Temp.:2-8°C 
  • Solubility.:H2O: 50 mg/mL 
  • XLogP3:0.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:206.141913202
  • Heavy Atom Count:15
  • Complexity:293
Purity/Quality:

98%min *data from raw suppliers

1-[4-(1-PYRROLIDINYL)-2-BUTYNYL]-2-PYRROLIDINONE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s): T+,
  • Hazard Codes:T+,C 
  • Statements: 28-34 
  • Safety Statements: 26-36/37/39-45 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCN(C1)CC#CCN2CCCC2=O
  • Clinical Use Nevertheless, oxotremorine, as a cholinergicagonist, facilitates memory storage. These findings haveserved as important leads in the development of agents usefulin treating Alzheimer disease. Although it possessesgroups that do not occur in other highly active muscarinicagents, oxotremorine’s trans conformation shows that distancesbetween possible active centers correspond with (+)-muscarine.
Technology Process of Oxotremorine

There total 2 articles about Oxotremorine 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 copper(l) chloride; In 1,4-dioxane; at 70 ℃; for 3h;
DOI:10.1021/jm00112a002
Guidance literature:
DOI:10.1021/jm00326a037 DOI:10.1021/jm00327a026
Guidance literature:
In ethanol;
Refernces Edit
Post RFQ for Price