N-(4-Iodophenyl)maleimide

Base Information

• Chemical Name: N-(4-Iodophenyl)maleimide
• CAS No.: 65833-01-4
• Molecular Formula: C10H6INO2
• Molecular Weight: 299.068
• Hs Code.: 2925190090
• European Community (EC) Number: 621-677-4
• NSC Number: 88871
• DSSTox Substance ID: DTXSID80216021
• Nikkaji Number: J847.567I
• Wikidata: Q83092151
• ChEMBL ID: CHEMBL579183
• Mol file: 65833-01-4.mol

Synonyms:N-(4-iodophenyl)maleimide

Chemical Property of N-(4-Iodophenyl)maleimide

Chemical Property:

• Vapor Pressure: 3.99E-06mmHg at 25°C
• Melting Point: 160
• Refractive Index: 1.705
• Boiling Point: 384.8 °C at 760 mmHg
• Flash Point: 186.5 °C
• PSA: 37.38000
• Density: 1.963 g/cm³
• LogP: 1.78560
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 298.94433
• Heavy Atom Count: 14
• Complexity: 275

Purity/Quality:

98%min ^*data from raw suppliers

N-(4-Iodophenyl)maleimide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC(=CC=C1N2C(=O)C=CC2=O)I

Technology Process of N-(4-Iodophenyl)maleimide

There total 6 articles about N-(4-Iodophenyl)maleimide 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: 69.0%

1-(4-iodophenyl)pyrrole (92636-36-7) → 1-(4-iodophenyl)-1H-pyrrole-2,5-dione (65833-01-4)

Guidance literature:

With oxygen; Rose Bengal lactone; In water; N,N-dimethyl-formamide; for 18h; Inert atmosphere; Irradiation;

DOI:10.1002/chem.201904168

Reference yield: 65.0%

maleic anhydride (108-31-6) + p-aminoiodobenzene (540-37-4) → 1-(4-iodophenyl)-1H-pyrrole-2,5-dione (65833-01-4)

Guidance literature:

maleic anhydride; p-aminoiodobenzene; In diethyl ether; at 20 ℃; for 2h;

With sodium acetate; acetic anhydride; at 120 ℃; for 4h;

DOI:10.1021/acs.orglett.9b03542

Reference yield:

(Z)-3-(4-Iodo-phenylcarbamoyl)-acrylic acid (17280-49-8,200706-68-9) → 1-(4-iodophenyl)-1H-pyrrole-2,5-dione (65833-01-4)

Guidance literature:

With sodium acetate; acetic anhydride; for 0.5h; Heating;

DOI:10.1021/jm900461w

upstream raw materials:

maleic anhydride

p-aminoiodobenzene

(Z)-3-(4-Iodo-phenylcarbamoyl)-acrylic acid

C₁₀H₈INO₃

Downstream raw materials:

(4aR,5aR,8aS,8bR)-2-{Bis-[1-(4-iodo-phenyl)-2,5-dioxo-pyrrolidin-3-yl]-methyl}-7-(4-iodo-phenyl)-4a-methyl-4a,5a,8a,8b-tetrahydro-pyrrolo[3',4':4,5]furo[3,2-b]pyridine-6,8-dione

3-{2-[(1-ethylpropylidene)hydrazono]-1-methylbutyl}-1-(4-iodophenyl)pyrrolidine-2,5-dione

3-[2-(cyclopentylidenehydrazono)cyclopentyl]-1-(4-iodophenyl)pyrrolidine-2,5-dione

2-(3,4,4a,5,6,7-hexahydro-3-oxo-2H-cyclopenta[c]pyridazin-4-yl)-N-(4-iodophenyl)acetamide

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