2-(2,4-dinitrophenyl)-1H-isoindole-1,3(2H)-dione

Base Information

• Chemical Name: 2-(2,4-dinitrophenyl)-1H-isoindole-1,3(2H)-dione
• CAS No.: 35843-60-8
• Molecular Formula: C14H7N3O6
• Molecular Weight: 313.2219
• Hs Code.: 2925190090
• Mol file: 35843-60-8.mol

Synonyms:N-(2,4-dinitro-phenyl)-phthalimide;2-(2,4-Dinitro-phenyl)-isoindole-1,3-dione;N-2,4-Dinitrobenzol-phthalimid;2-(2,4-Dinitrophenyl)-1H-isoindole-1,3(2H)-dione;1H-Isoindole-1,3(2H)-dione,2-(2,4-dinitrophenyl);

Chemical Property of 2-(2,4-dinitrophenyl)-1H-isoindole-1,3(2H)-dione

Chemical Property:

• Vapor Pressure: 5.83E-12mmHg at 25°C
• Boiling Point: 545.6°Cat760mmHg
• Flash Point: 283.8°C
• PSA: 129.02000
• Density: 1.644g/cm³
• LogP: 3.41500

Purity/Quality:

99%, ^*data from raw suppliers

2-(2,4-Dinitrophenyl)isoindole-1,3-dione 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-(2,4-dinitrophenyl)-1H-isoindole-1,3(2H)-dione

There total 4 articles about 2-(2,4-dinitrophenyl)-1H-isoindole-1,3(2H)-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:

potassium phtalimide (1074-82-4) + 1-chloro-2,4-dinitro-benzene (97-00-7) → N-2,4-Dinitrobenzol-phthalimid (35843-60-8)

Guidance literature:

at 200 ℃;

Reference yield:

phthalic anhydride (85-44-9) + 2,4-Dinitroanilin (97-02-9) → N-2,4-Dinitrobenzol-phthalimid (35843-60-8)

Guidance literature:

at 260 ℃;

Reference yield:

2,4-Dinitrofluorobenzene (70-34-8,65727-75-5) + potassium phtalimide (1074-82-4) → N-2,4-Dinitrobenzol-phthalimid (35843-60-8)

Guidance literature:

With acetone;

upstream raw materials:

phthalic anhydride

2,4-Dinitroanilin

2,4-Dinitrofluorobenzene

potassium phtalimide