Benzo[f]quinolin-3(4H)-one

Base Information

Chemical Name:Benzo[f]quinolin-3(4H)-one
CAS No.:23981-08-0
Molecular Formula:C13H9NO
Molecular Weight:195.221
Hs Code.:2933990090
DSSTox Substance ID:DTXSID60383008
Nikkaji Number:J88.218F
Wikidata:Q82174543
Mol file:23981-08-0.mol

Synonyms:Benzo[f]quinolin-3(4H)-one;23981-08-0;benzo[f]quinoline-3(4h)-one;SCHEMBL3847120;DTXSID60383008;AKOS006295620;3H,4H-BENZO[F]QUINOLIN-3-ONE

Suppliers and Price of Benzo[f]quinolin-3(4H)-one

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 3 raw suppliers

Chemical Property of Benzo[f]quinolin-3(4H)-one

Chemical Property:

PSA：33.12000
LogP:3.09360
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:195.068413911
Heavy Atom Count:15
Complexity:297

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC3=C2C=CC(=O)N3

Technology Process of Benzo[f]quinolin-3(4H)-one

There total 7 articles about Benzo[f]quinolin-3(4H)-one 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: 84.0%

: C₂₀H₁₀F₅NO₂

: 23981-08-0
benzoquinolin-1(2H)-one

Guidance literature:: C₂₀H₁₀F₅NO₂; With di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; toluene;

With dichloro( 1,5-cyclooctadiene)platinum(ll); diallylcarbonate; silver trifluoroacetate; In dichloromethane; toluene; at 20 ℃; for 24h; chemoselective reaction; Sealed tube;
DOI:10.1002/anie.201811197