1,10-Phenanthroline 1,10-dioxide

Base Information

Chemical Name:1,10-Phenanthroline 1,10-dioxide
CAS No.:72799-24-7
Molecular Formula:C12H8N2O2
Molecular Weight:212.208
Hs Code.:
DSSTox Substance ID:DTXSID00451295
Nikkaji Number:J1.275.425F
Wikidata:Q82271250

Synonyms:1,10-Phenanthroline 1,10-dioxide;72799-24-7;1,10-Phenanthroline, 1,10-dioxide;starbld0013276;SCHEMBL5352485;DTXSID00451295;1,10-phenanthroline N,N'-dioxide

Suppliers and Price of 1,10-Phenanthroline 1,10-dioxide

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
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price

Total 15 raw suppliers

Chemical Property of 1,10-Phenanthroline 1,10-dioxide

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:212.058577502
Heavy Atom Count:16
Complexity:512

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CN(C2=C3C(=CC=C[N+]3=O)C=CC2=C1)[O-]
General Description 1,10-Phenanthroline, 1,10-dioxide, also known as 1,10-phenanthroline N,N′-dioxide, is a derivative of 1,10-phenanthroline where both nitrogen atoms are oxidized to form N-oxide functional groups. 1,10-Phenanthroline, 1,10-dioxide can be efficiently synthesized using HOF·CH₃CN as an oxygen-transfer agent, yielding the dioxide product in high efficiency and short reaction times. The oxidation process is selective for the nitrogen atoms, preserving the aromatic framework of the phenanthroline core. The resulting 1,10-phenanthroline dioxide is of interest due to its potential applications in coordination chemistry and as a ligand or intermediate in synthetic organic chemistry.

Technology Process of 1,10-Phenanthroline 1,10-dioxide

There total 3 articles about 1,10-Phenanthroline 1,10-dioxide 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:

Reference yield: 60.0%