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5-azoniaspiro[4.4]nonane

Base Information Edit
  • Chemical Name:5-azoniaspiro[4.4]nonane
  • CAS No.:16450-38-7
  • Molecular Formula:C8H16 N . Br
  • Molecular Weight:206.126
  • Hs Code.:
  • European Community (EC) Number:835-166-0
  • DSSTox Substance ID:DTXSID80466504
  • NSC Number:28372
  • Mol file:16450-38-7.mol
5-azoniaspiro[4.4]nonane

Synonyms:5-Azoniaspiro[4.4]nonane,bromide (6CI,7CI,8CI,9CI); 1,1'-Spirobipyrrolidinium bromide

Suppliers and Price of 5-azoniaspiro[4.4]nonane
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 8 raw suppliers
Chemical Property of 5-azoniaspiro[4.4]nonane Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:g/cm3 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:205.04661
  • Heavy Atom Count:10
  • Complexity:79.6
Purity/Quality:

98%,99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC[N+]2(C1)CCCC2.[Br-]
Technology Process of 5-azoniaspiro[4.4]nonane

There total 6 articles about 5-azoniaspiro[4.4]nonane 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 resin Amberlite A26; In acetonitrile; for 6h; Solvent; Temperature; Time; Reflux;
Guidance literature:
With ammonium hydroxide; In 2-methyltetrahydrofuran; at 30 ℃; for 9h;
Guidance literature:
With sodium hydroxide;
DOI:10.1021/jo01353a004
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