3-Chloro-4-(4-methylphenyl)-1-phenyl-1H-pyrrole-2,5-dione

Base Information

Chemical Name:3-Chloro-4-(4-methylphenyl)-1-phenyl-1H-pyrrole-2,5-dione
CAS No.:74211-55-5
Molecular Formula:C17H12ClNO2
Molecular Weight:297.741
Hs Code.:
DSSTox Substance ID:DTXSID80502310
Wikidata:Q82355223

Synonyms:74211-55-5;DTXSID80502310;3-Chloro-4-(4-methylphenyl)-1-phenyl-1H-pyrrole-2,5-dione

Suppliers and Price of 3-Chloro-4-(4-methylphenyl)-1-phenyl-1H-pyrrole-2,5-dione

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 3-Chloro-4-(4-methylphenyl)-1-phenyl-1H-pyrrole-2,5-dione

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:297.0556563
Heavy Atom Count:21
Complexity:471

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C2=C(C(=O)N(C2=O)C3=CC=CC=C3)Cl

Technology Process of 3-Chloro-4-(4-methylphenyl)-1-phenyl-1H-pyrrole-2,5-dione

There total 2 articles about 3-Chloro-4-(4-methylphenyl)-1-phenyl-1H-pyrrole-2,5-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: 83.0%

: 87292-74-8
1-(4-Methylphenyl)-2-chlor-maleinsaeureanhydrid

: 62-53-3
aniline

: 74211-55-5
2-(4-Methylphenyl)-3-chlor-N-phenyl-maleinimid

Guidance literature:: In acetic acid; for 2h; Heating;

Reference yield:

: 3152-16-7
1-(4-Methylphenyl)maleinsaeureanhydrid

: 74211-55-5
2-(4-Methylphenyl)-3-chlor-N-phenyl-maleinimid

Guidance literature:: Multi-step reaction with 2 steps

1: 53 percent / SOCl₂, pyridine / 0.17 h / 75 °C / Heating

2: 83 percent / acetic acid / 2 h / Heating

With pyridine; thionyl chloride; In acetic acid;