3,4-Dibromo-1-phenylpyrrolidine-2,5-dione

Base Information

Chemical Name:3,4-Dibromo-1-phenylpyrrolidine-2,5-dione
CAS No.:58879-90-6
Molecular Formula:C10H7Br2NO2
Molecular Weight:332.979
Hs Code.:
DSSTox Substance ID:DTXSID00534138

Synonyms:3,4-Dibromo-1-phenylpyrrolidine-2,5-dione;58879-90-6;SCHEMBL17236309;DTXSID00534138;1-phenyl-3,4-dibromopyrroline-2,5-dione

Suppliers and Price of 3,4-Dibromo-1-phenylpyrrolidine-2,5-dione

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

Total 6 raw suppliers

Chemical Property of 3,4-Dibromo-1-phenylpyrrolidine-2,5-dione

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:332.88230
Heavy Atom Count:15
Complexity:269

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 3,4-Dibromo-1-phenylpyrrolidine-2,5-dione

There total 5 articles about 3,4-Dibromo-1-phenylpyrrolidine-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: 91.0%

: 941-69-5
N-phenyl-maleimide

: 58879-90-6
3,4-dibromo-1-phenylpyrrolidine-2,5-dione

Guidance literature:: With bromine; In tetrachloromethane; for 1h; Inert atmosphere; Reflux;
DOI:10.1021/acs.joc.5b02036

Reference yield:

: 62-53-3
aniline

: 58879-90-6
3,4-dibromo-1-phenylpyrrolidine-2,5-dione

Guidance literature:: Multi-step reaction with 2 steps

1: benzene

2: acetyl chloride

With acetyl chloride; benzene;

Reference yield:

: 37902-58-2
3-phenylcarbamoylacrylic acid

: 58879-90-6
3,4-dibromo-1-phenylpyrrolidine-2,5-dione

Guidance literature:: Multi-step reaction with 2 steps

1: sodium acetate; acetic anhydride / 16 h / 70 °C / Inert atmosphere

2: bromine / tetrachloromethane / 2 h / Inert atmosphere; Reflux

With bromine; sodium acetate; acetic anhydride; In tetrachloromethane;
DOI:10.1002/anie.201609733