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1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione

Base Information
  • Chemical Name:1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione
  • CAS No.:1082-85-5
  • Molecular Formula:C12H9NO3
  • Molecular Weight:215.208
  • Hs Code.:2925190090
  • European Community (EC) Number:214-106-1
  • NSC Number:209075
  • UNII:PPX4Y26HKM
  • DSSTox Substance ID:DTXSID10148462
  • Nikkaji Number:J217.207K
  • Wikidata:Q69757165
  • Mol file:1082-85-5.mol
1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione

Synonyms:1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione;1082-85-5;n-(4-acetylphenyl)maleimide;1-(4-acetylphenyl)pyrrole-2,5-dione;PPX4Y26HKM;EINECS 214-106-1;NSC-209075;1-(4-acetylphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione;N-(4-Acetylphenyl)Maleinimide;MFCD00014537;NSC209075;Cyto8G9;p-maleimidoacetophenone;UNII-PPX4Y26HKM;CBMicro_026329;N-(p-Acetylphenyl)maleimide;SCHEMBL371252;DTXSID10148462;BBL018919;STL015405;AKOS000296063;NSC 209075;1-(4-acetylphenyl)-pyrrole-2,5-dione;BIM-0026282.P001;FT-0629194;EN300-17192;D95959;AB00673634-01;6T-0056;A801836;J-503222;Z56899062

Suppliers and Price of 1-(4-Acetylphenyl)-1H-pyrrole-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
  • TRC
  • 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione
  • 100mg
  • $ 75.00
  • SynQuest Laboratories
  • N-(4-Acetylphenyl)maleimide 98%
  • 5 g
  • $ 288.00
  • SynQuest Laboratories
  • N-(4-Acetylphenyl)maleimide 98%
  • 1 g
  • $ 72.00
  • Matrix Scientific
  • 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione >95%
  • 500mg
  • $ 181.00
  • Matrix Scientific
  • 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione >95%
  • 1g
  • $ 228.00
  • Matrix Scientific
  • 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione >95%
  • 5g
  • $ 524.00
  • Crysdot
  • 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione 95+%
  • 25g
  • $ 547.00
  • Chemenu
  • 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione 95%
  • 25g
  • $ 516.00
  • Biosynth Carbosynth
  • N-(4-Acetylphenyl)maleimide
  • 100 g
  • $ 308.00
  • Biosynth Carbosynth
  • N-(4-Acetylphenyl)maleimide
  • 250 g
  • $ 655.00
Total 26 raw suppliers
Chemical Property of 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione
Chemical Property:
  • Vapor Pressure:1.01E-06mmHg at 25°C 
  • Melting Point:153-156 °C 
  • Refractive Index:1.613 
  • Boiling Point:403.6 °C at 760 mmHg 
  • PKA:-3.77±0.20(Predicted) 
  • Flash Point:195.6 °C 
  • PSA:54.45000 
  • Density:1.33 g/cm3 
  • LogP:1.38360 
  • Water Solubility.:Insoluble in water. 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:215.058243149
  • Heavy Atom Count:16
  • Complexity:347
Purity/Quality:

97% *data from raw suppliers

1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXnIrritantXi 
  • Hazard Codes:Xn,Xi 
  • Statements: 36/37/38-22 
  • Safety Statements: 37/39-26 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)C1=CC=C(C=C1)N2C(=O)C=CC2=O
  • Uses N-(4-Acetylphenyl)maleimide is used as cross linking agent for reversible conjugation of thiol- containing compounds.
Technology Process of 1-(4-Acetylphenyl)-1H-pyrrole-2,5-dione

There total 6 articles about 1-(4-Acetylphenyl)-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:
Guidance literature:
With acetic acid; for 2h; Reflux;
DOI:10.1016/j.bmcl.2020.127655
Guidance literature:
With aluminium trichloride; In nitrobenzene; at 0 ℃; for 3h;
DOI:10.1007/BF00954385
Guidance literature:
With sodium acetate; acetic anhydride; at 75 ℃;
DOI:10.1016/j.bmcl.2010.01.098
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