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1-Azacyclohexadecane

Base Information
  • Chemical Name:1-Azacyclohexadecane
  • CAS No.:295-66-9
  • Molecular Formula:C15H31N
  • Molecular Weight:225.418
  • Hs Code.:
  • Mol file:295-66-9.mol
1-Azacyclohexadecane

Synonyms:Pentadecamethylenimine

Suppliers and Price of 1-Azacyclohexadecane
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
Total 4 raw suppliers
Chemical Property of 1-Azacyclohexadecane
Chemical Property:
  • PSA:12.03000 
  • LogP:4.98970 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1-Azacyclohexadecane

There total 5 articles about 1-Azacyclohexadecane 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 lithium aluminium tetrahydride; In diethyl ether;
DOI:10.1021/jo01308a002
Guidance literature:
Multi-step reaction with 3 steps
1: NH2OH; sodium acetate / methanol / 1 h / 20 °C
2: pyridine; tosyl chloride / CH2Cl2 / 20 °C
3: LiAlH4 / tetrahydrofuran / 16 h / 70 °C
With pyridine; lithium aluminium tetrahydride; hydroxylamine; sodium acetate; p-toluenesulfonyl chloride; In tetrahydrofuran; methanol; dichloromethane; 2: Beckman rearrangement;
DOI:10.1021/jo016101c
Guidance literature:
Multi-step reaction with 2 steps
1: pyridine; tosyl chloride / CH2Cl2 / 20 °C
2: LiAlH4 / tetrahydrofuran / 16 h / 70 °C
With pyridine; lithium aluminium tetrahydride; p-toluenesulfonyl chloride; In tetrahydrofuran; dichloromethane; 1: Beckman rearrangement;
DOI:10.1021/jo016101c
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