3-methoxy-1-phenyl-1H-pyrrole-2,5-dione

Base Information

Chemical Name:3-methoxy-1-phenyl-1H-pyrrole-2,5-dione
CAS No.:558473-96-4
Molecular Formula:C11H9NO3
Molecular Weight:203.197
Hs Code.:
DSSTox Substance ID:DTXSID50464719
Nikkaji Number:J1.903.812B
Wikidata:Q82290168

Synonyms:558473-96-4;3-methoxy-1-phenyl-1H-pyrrole-2,5-dione;3-methoxy-1-phenylpyrrole-2,5-dione;3-methoxy-1-phenyl-pyrrole-2,5-dione;1H-Pyrrole-2,5-dione, 3-methoxy-1-phenyl-;DTXSID50464719

Suppliers and Price of 3-methoxy-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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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of 3-methoxy-1-phenyl-1H-pyrrole-2,5-dione

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:203.058243149
Heavy Atom Count:15
Complexity:316

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC(=O)N(C1=O)C2=CC=CC=C2

Technology Process of 3-methoxy-1-phenyl-1H-pyrrole-2,5-dione

There total 5 articles about 3-methoxy-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: 75.0%

: 67-56-1
methanol

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

: 558473-96-4
2-methoxy-N-phenylmaleimide

Guidance literature:: With triethylamine; for 1h; Heating;
DOI:10.1055/s-2003-37351

Reference yield:

: 941-69-5
N-phenyl-maleimide

: 558473-96-4
2-methoxy-N-phenylmaleimide

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / Br₂ / CCl₄ / 1 h / Heating

2: 98 percent / Et₃N / tetrahydrofuran / 2 h / 0 °C

3: 75 percent / Et₃N / 1 h / Heating

With bromine; triethylamine; In tetrahydrofuran; tetrachloromethane;
DOI:10.1055/s-2003-37351

Reference yield:

: trans-2,3-dibromo-N-phenylsuccinimide

: 558473-96-4
2-methoxy-N-phenylmaleimide

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / Et₃N / tetrahydrofuran / 2 h / 0 °C

2: 75 percent / Et₃N / 1 h / Heating

With triethylamine; In tetrahydrofuran;
DOI:10.1055/s-2003-37351