1-Phenyl-3-(phenylsulfanyl)-1H-pyrrole-2,5-dione

Base Information

Chemical Name:1-Phenyl-3-(phenylsulfanyl)-1H-pyrrole-2,5-dione
CAS No.:103056-32-2
Molecular Formula:C16H11NO2S
Molecular Weight:281.335
Hs Code.:
DSSTox Substance ID:DTXSID30562500
Nikkaji Number:J282.570H
Wikidata:Q82446690
Mol file:103056-32-2.mol

Synonyms:103056-32-2;1-Phenyl-3-(phenylsulfanyl)-1H-pyrrole-2,5-dione;SCHEMBL9615534;DTXSID30562500

Suppliers and Price of 1-Phenyl-3-(phenylsulfanyl)-1H-pyrrole-2,5-dione

Supply Marketing:

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

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Chemical Property of 1-Phenyl-3-(phenylsulfanyl)-1H-pyrrole-2,5-dione

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:281.05104977
Heavy Atom Count:20
Complexity:420

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)N2C(=O)C=C(C2=O)SC3=CC=CC=C3

Technology Process of 1-Phenyl-3-(phenylsulfanyl)-1H-pyrrole-2,5-dione

There total 6 articles about 1-Phenyl-3-(phenylsulfanyl)-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: 96.0%

: 72000-67-0
3-bromo-1-phenyl-1H-pyrrole-2,5-dione

: 108-98-5
thiophenol

: 103056-32-2
3-phenylthio-1-phenyl-1H-pyrrole-2,5-dione

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 1h; Inert atmosphere;

Reference yield: 85.0%

: 144328-37-0
2-chloro-N-phenyl-2-(phenylthio)succinimide

: 103056-32-2
3-phenylthio-1-phenyl-1H-pyrrole-2,5-dione

Guidance literature:: at 110 - 150 ℃; for 0.166667h;
DOI:10.1016/0040-4020(95)00735-Q

Reference yield:

: 941-69-5
N-phenyl-maleimide

: 103056-32-2
3-phenylthio-1-phenyl-1H-pyrrole-2,5-dione

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / Et₃N / benzene

2: 70 percent / N-chlorosuccinimide / CCl₄ / 12 h / Heating

3: 85 percent / 0.17 h / 110 - 150 °C

With N-chloro-succinimide; triethylamine; In tetrachloromethane; benzene;
DOI:10.1016/0040-4020(95)00735-Q