2,4,9-Triphenyl-5,6-dihydrobenzo[h]quinoline

Base Information

Chemical Name:2,4,9-Triphenyl-5,6-dihydrobenzo[h]quinoline
CAS No.:88065-00-3
Molecular Formula:C₃₁H₂₃N
Molecular Weight:409.53
Hs Code.:
DSSTox Substance ID:DTXSID60394538
Wikidata:Q82193988

Synonyms:2,4,9-triphenyl-5,6-dihydrobenzo[h]quinoline;88065-00-3;DTXSID60394538

Suppliers and Price of 2,4,9-Triphenyl-5,6-dihydrobenzo[h]quinoline

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 0 raw suppliers

Chemical Property of 2,4,9-Triphenyl-5,6-dihydrobenzo[h]quinoline

Chemical Property:

Boiling Point:600.2±54.0 °C(Predicted)
PSA：12.89000
Density:1.153±0.06 g/cm3(Predicted)
LogP:7.84820
XLogP3:7.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:409.183049738
Heavy Atom Count:32
Complexity:581

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2=C(C3=C1C=CC(=C3)C4=CC=CC=C4)N=C(C=C2C5=CC=CC=C5)C6=CC=CC=C6

Technology Process of 2,4,9-Triphenyl-5,6-dihydrobenzo[h]quinoline

There total 3 articles about 2,4,9-Triphenyl-5,6-dihydrobenzo[h]quinoline 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:

: 88064-97-5
5,6-dihydro-2,4,9-triphenylbenzochromelium trifluoromethanesulphonate

: 88065-00-3
5,6-dihydro-2,4,9-triphenylbenzoquinoline

Guidance literature:: With ammonium hydroxide; acetic acid; Yield given. Multistep reaction; 1) Et₂O, 2 h; 2) Et₂O, 16 h;
DOI:10.1039/P29830001455

Reference yield:

: 41526-73-2
7-phenyl-3,4-dihydronaphthalen-1(2H)-one

: 88065-00-3
5,6-dihydro-2,4,9-triphenylbenzoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / 2 h / 100 °C

2: 1) aqueous NH₃; 2) AcOH / 1) Et₂O, 2 h; 2) Et₂O, 16 h

With ammonium hydroxide; acetic acid;
DOI:10.1039/P29830001455