5,6-dibroMoisoindoline-1,3-dione

Base Information

• Chemical Name: 5,6-dibroMoisoindoline-1,3-dione
• CAS No.: 247045-28-9
• Molecular Formula: C8H3Br2NO2
• Molecular Weight: 304.925
• Hs Code.: 2925190090
• Mol file: 247045-28-9.mol

Synonyms:5,6-dibromo-isoindoline-1,3-dione;5,6-Dibrom-isoindolin-1,3-dion;4,5-dibromophthalimide;

Chemical Property of 5,6-dibroMoisoindoline-1,3-dione

Chemical Property:

• Melting Point: 235-240 °C(Solv: ethanol (64-17-5); water (7732-18-5))
• PKA: 8.29±0.20(Predicted)
• PSA: 49.66000
• Density: 2.179±0.06 g/cm3(Predicted)
• LogP: 2.10560
• Storage Temp.: Sealed in dry,Room Temperature

Purity/Quality:

97% ^*data from raw suppliers

5,6-Dibromoisoindoline-1,3-dione 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 5,6-dibroMoisoindoline-1,3-dione

There total 5 articles about 5,6-dibroMoisoindoline-1,3-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: 96.0%

4,5-dibromophthalic anhydride (65237-17-4) → 4,5-dibromophthalimide (247045-28-9)

Guidance literature:

With urea; at 180 ℃; for 2h;

DOI:10.1002/(SICI)1099-0690(200001)2000:2<303::AID-EJOC303>3.0.CO;2-M

Reference yield:

4,5-dibromophthalic acid (24063-28-3) → 4,5-dibromophthalimide (247045-28-9)

Guidance literature:

With ammonium acetate; In acetic acid;

DOI:10.1021/ja209589x

Reference yield:

→ 4,5-dibromophthalimide (247045-28-9)

Guidance literature:

With ammonia; in Schmelze;

upstream raw materials:

4,5-dibromo-phthalamic acid

4,5-dibromophthalic anhydride

4,5-dibromophthalic acid

Downstream raw materials:

2-amino-4,5-dibromobenzoic acid

4,5-dicyanophthalimide

pyrrolo[3,4-f]isoindole-1,3,5,7-tetraone

4,5-dibromophthalic acid