1-(4-Nitrobenzoyl)-9H-indeno[2,1-B]pyridin-1-ium chloride

Base Information

Chemical Name:1-(4-Nitrobenzoyl)-9H-indeno[2,1-B]pyridin-1-ium chloride
CAS No.:88091-79-6
Molecular Formula:C₁₉H₁₃N₂O₃*Cl
Molecular Weight:352.777
Hs Code.:
DSSTox Substance ID:DTXSID90521370

Synonyms:88091-79-6;DTXSID90521370;1-(4-NITROBENZOYL)-9H-INDENO[2,1-B]PYRIDIN-1-IUM CHLORIDE

Suppliers and Price of 1-(4-Nitrobenzoyl)-9H-indeno[2,1-B]pyridin-1-ium chloride

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 0 raw suppliers

Chemical Property of 1-(4-Nitrobenzoyl)-9H-indeno[2,1-B]pyridin-1-ium chloride

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:352.0614700
Heavy Atom Count:25
Complexity:495

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2=CC=CC=C2C3=C1[N+](=CC=C3)C(=O)C4=CC=C(C=C4)[N+](=O)[O-].[Cl-]

Technology Process of 1-(4-Nitrobenzoyl)-9H-indeno[2,1-B]pyridin-1-ium chloride

There total 2 articles about 1-(4-Nitrobenzoyl)-9H-indeno[2,1-B]pyridin-1-ium chloride 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: 65.0%

: 244-44-0
1-azafluorene

: 122-04-3
4-nitro-benzoyl chloride

: 88091-79-6
N-(p-nitrobenzoyl)-1-azafluorenium chloride

Guidance literature:: In benzene; at 20 ℃; for 16h; 1 hr. 80 deg C;
DOI:10.1007/BF00516458

Reference yield:

: 88091-78-5
N-benzoyl-1-azafluorenium chloride

: 88091-79-6
N-(p-nitrobenzoyl)-1-azafluorenium chloride

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / H₂O / triethylamine

2: 65 percent / benzene / 16 h / 20 °C / 1 hr. 80 deg C

With potassium hydroxide; In water; benzene;
DOI:10.1007/BF00516458