3,4-Dihydro-9-phenyl-1(2H)-acridinone

Base Information

Chemical Name:3,4-Dihydro-9-phenyl-1(2H)-acridinone
CAS No.:17401-27-3
Molecular Formula:C19H15NO
Molecular Weight:273.334
Hs Code.:2933990090
ChEMBL ID:CHEMBL3945975
DSSTox Substance ID:DTXSID10429288
Nikkaji Number:J1.264.319E
Wikidata:Q82242289
Mol file:17401-27-3.mol

Synonyms:3,4-Dihydro-9-phenyl-1(2H)-acridinone;17401-27-3;9-phenyl-3,4-dihydro-2H-acridin-1-one;9-Phenyl-3,4-dihydroacridin-1(2H)-one;starbld0008048;CHEMBL3945975;DTXSID10429288;AKOS033817136;NCGC00320698-01;CS-0269787;FT-0667033;AB00985185-01;AB00985185-03;T5728418;Z223687154

Suppliers and Price of 3,4-Dihydro-9-phenyl-1(2H)-acridinone

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

TRC
3,4-Dihydro-9-phenyl-1(2H)-acridinone
5g
$ 1100.00

Total 17 raw suppliers

Chemical Property of 3,4-Dihydro-9-phenyl-1(2H)-acridinone

Chemical Property:

PSA：29.96000
LogP:4.42080
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:273.115364102
Heavy Atom Count:21
Complexity:387

Purity/Quality:

99% ,98%,Electron Grade , ^*data from raw suppliers

3,4-Dihydro-9-phenyl-1(2H)-acridinone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=NC3=CC=CC=C3C(=C2C(=O)C1)C4=CC=CC=C4
Uses 3,4-Dihydro-9-phenyl-1(2H)-acridinone is used in the Friedlander synthesis of quinolines.

Technology Process of 3,4-Dihydro-9-phenyl-1(2H)-acridinone

There total 5 articles about 3,4-Dihydro-9-phenyl-1(2H)-acridinone 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: 100.0%

: 504-02-9
1,3-cylohexanedione

: 2835-77-0
(2-aminophenyl)(phenyl)methanone

: 17401-27-3
9-phenyl-3,4-dihydro-2H-acridin-1-one

Guidance literature:: With o-benzenedisulfonimide; at 80 ℃; for 4h; Neat (no solvent);
DOI:10.1016/j.tetlet.2010.02.139

Reference yield: 91.0%

: 13047-06-8
o-bromobenzophenone

: 504-02-9
1,3-cylohexanedione

: 17401-27-3
9-phenyl-3,4-dihydro-2H-acridin-1-one

Guidance literature:: With D-glucose; copper(II) sulfate; L-proline; potassium hydroxide; In ethanol; water; at 90 ℃; for 4h;
DOI:10.1039/c4ra14138e

Reference yield: 68.0%

: 108-94-1,11119-77-0,9003-41-2,9075-99-4
cyclohexanone

: 2835-77-0
(2-aminophenyl)(phenyl)methanone

: 17401-27-3
9-phenyl-3,4-dihydro-2H-acridin-1-one

Guidance literature:: With Cu(II) decorated on isoniazid functionalized silica coated Fe₃O₄ magnetic nanoparticles; In ethanol; at 60 ℃; for 2h;
DOI:10.1016/j.poly.2019.114148