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10-Methyl-1,4,7-trioxa-10-azacyclododecan-10-ium

Base Information Edit
  • Chemical Name:10-Methyl-1,4,7-trioxa-10-azacyclododecan-10-ium
  • CAS No.:69978-45-6
  • Molecular Formula:C9H19 N O3
  • Molecular Weight:189.255
  • Hs Code.:29349990
  • DSSTox Substance ID:DTXSID70990227
  • Wikidata:Q82979611
  • Mol file:69978-45-6.mol
10-Methyl-1,4,7-trioxa-10-azacyclododecan-10-ium

Synonyms:DTXSID70990227;10-methyl-1,4,7-trioxa-10-azacyclododecan-10-ium

Suppliers and Price of 10-Methyl-1,4,7-trioxa-10-azacyclododecan-10-ium
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
Total 9 raw suppliers
Chemical Property of 10-Methyl-1,4,7-trioxa-10-azacyclododecan-10-ium Edit
Chemical Property:
  • Vapor Pressure:0.00595mmHg at 25°C 
  • Refractive Index:1.468-1.47 
  • Boiling Point:272.8°C at 760 mmHg 
  • Flash Point:79.6°C 
  • PSA:30.93000 
  • Density:1.0930 (rough estimate) 
  • LogP:-0.08050 
  • XLogP3:-0.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:190.14431850
  • Heavy Atom Count:13
  • Complexity:109
Purity/Quality:

98%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C[NH+]1CCOCCOCCOCC1
Technology Process of 10-Methyl-1,4,7-trioxa-10-azacyclododecan-10-ium

There total 7 articles about 10-Methyl-1,4,7-trioxa-10-azacyclododecan-10-ium 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:
Multi-step reaction with 4 steps
1: NaI / acetone / 70 h / Heating
2: 54 percent / Na2CO3 / acetonitrile / 18 h / Heating
3: 85 percent / H2 / Pd/C / acetic acid / 15 h / 60 °C / 2280 Torr
4: 1.) K2CO3, 2.) LiAlH4 / 1.) THF, 2.) RT, 18 h
With lithium aluminium tetrahydride; hydrogen; sodium carbonate; potassium carbonate; sodium iodide; palladium on activated charcoal; In acetic acid; acetone; acetonitrile;
Guidance literature:
Multi-step reaction with 5 steps
1: 83 percent / thionyl chloride / pyridine / Ambient temperature
2: NaI / acetone / 70 h / Heating
3: 54 percent / Na2CO3 / acetonitrile / 18 h / Heating
4: 85 percent / H2 / Pd/C / acetic acid / 15 h / 60 °C / 2280 Torr
5: 1.) K2CO3, 2.) LiAlH4 / 1.) THF, 2.) RT, 18 h
With lithium aluminium tetrahydride; thionyl chloride; hydrogen; sodium carbonate; potassium carbonate; sodium iodide; palladium on activated charcoal; In pyridine; acetic acid; acetone; acetonitrile;
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