4-(2-Methoxyphenyl)-2-methyl-1H-benzo[f]isoindole-1,3(2H)-dione

Base Information

Chemical Name:4-(2-Methoxyphenyl)-2-methyl-1H-benzo[f]isoindole-1,3(2H)-dione
CAS No.:92755-92-5
Molecular Formula:C₂₀H₁₅NO₃
Molecular Weight:317.344
Hs Code.:
DSSTox Substance ID:DTXSID90534662
Wikidata:Q82408598

Synonyms:92755-92-5;DTXSID90534662;4-(2-Methoxyphenyl)-2-methyl-1H-benzo[f]isoindole-1,3(2H)-dione

Suppliers and Price of 4-(2-Methoxyphenyl)-2-methyl-1H-benzo[f]isoindole-1,3(2H)-dione

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 4-(2-Methoxyphenyl)-2-methyl-1H-benzo[f]isoindole-1,3(2H)-dione

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:317.10519334
Heavy Atom Count:24
Complexity:519

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C(=O)C2=CC3=CC=CC=C3C(=C2C1=O)C4=CC=CC=C4OC

Technology Process of 4-(2-Methoxyphenyl)-2-methyl-1H-benzo[f]isoindole-1,3(2H)-dione

There total 3 articles about 4-(2-Methoxyphenyl)-2-methyl-1H-benzo[f]isoindole-1,3(2H)-dione 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:

: 69927-55-5,69979-94-8
endo N-methyl(hydroxy-2 phenyl)-1 epoxy-1,4 tetrahydro-1,2,3,4 naphthalenedicarboximide-2,3

: 92755-92-5
N-methyl(methoxy-2 phenyl)-1 naphthalenedicarboximide-2,3

Guidance literature:: Multi-step reaction with 3 steps

1: 62 percent / CF₃COOH / CDCl₃ / 0.5 h

2: 74 percent / 0.08 h / 250 °C

3: diethyl ether / 1 h

With trifluoroacetic acid; In diethyl ether; chloroform-d1;