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4,5-DICHLOROPHTHALIMIDE

Base Information
  • Chemical Name:4,5-DICHLOROPHTHALIMIDE
  • CAS No.:15997-89-4
  • Molecular Formula:C8H3Cl2NO2
  • Molecular Weight:216.023
  • Hs Code.:2925190090
  • Mol file:15997-89-4.mol
4,5-DICHLOROPHTHALIMIDE

Synonyms:5,6-Dichloroisoindoline-1,3-dione;5,6-Dichloro-2H-benzo[c]azoline-1,3-dione;4,5-Dichlorophthalimide;

Suppliers and Price of 4,5-DICHLOROPHTHALIMIDE
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
  • 4,5-Dichlorophthalimide
  • 100mg
  • $ 75.00
  • Sigma-Aldrich
  • 4,5-Dichlorophthalimide 97%
  • 5g
  • $ 61.30
  • Crysdot
  • 5,6-Dichloroisoindoline-1,3-dione 95+%
  • 10g
  • $ 486.00
  • American Custom Chemicals Corporation
  • 4,5-DICHLOROPHTHALIMIDE 95.00%
  • 5G
  • $ 844.68
  • Alichem
  • 5,6-Dichloroisoindoline-1,3-dione
  • 10g
  • $ 520.46
  • Alichem
  • 5,6-Dichloroisoindoline-1,3-dione
  • 5g
  • $ 342.10
  • AK Scientific
  • 5,6-Dichloroisoindoline-1,3-dione
  • 1g
  • $ 179.00
Total 16 raw suppliers
Chemical Property of 4,5-DICHLOROPHTHALIMIDE
Chemical Property:
  • Melting Point:217-219 °C(lit.) 
  • Refractive Index:1.637 
  • PKA:7.84±0.20(Predicted) 
  • PSA:46.17000 
  • Density:1.643 g/cm3 
  • LogP:2.20580 
  • Storage Temp.:2-8°C 
Purity/Quality:

97% *data from raw suppliers

4,5-Dichlorophthalimide *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Uses 4,5-Dichlorophthalimide (5,6-dichloro-1H-isoindole-1,3(2H)-dione) is suitable as a reactant in the synthesis of 5′-N-(4′′,5′′-dichlorophthaloyl)-3′-azido-2′,3′-dideoxythymidine and 2-amino-4,5-dichlorobenzoic acid.It may be used in the following studies:As a reactant in the synthesis of 4,5-dichloro-1,2-benzenedicarboxamide.As an additive in the Ir-BICP catalyzed asymmetric hydrogenation of 2,3,3-trimethylindolenine to improve enantioselectivity.As a reactant in the synthesis of octachloro-Cu-phthalocyanine.As a reagent in the synthesis of 7-tert-butylthianthrene-2,3-dicarboxylic imide.As a starting material in the synthesis of N-(3-bromopropyl)-4,5-dichlorophthalimide.As a nucleophilic partner in the phosphine-catalyzed allylic substitution of Morita-Baylis-Hillman acetates to form N-protected β-amino phosphonic acid esters.
Technology Process of 4,5-DICHLOROPHTHALIMIDE

There total 6 articles about 4,5-DICHLOROPHTHALIMIDE 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 formamide; at 180 - 190 ℃;
DOI:10.1016/j.ejmech.2012.06.020
Guidance literature:
With formamide; at 140 - 180 ℃; for 4h;
DOI:10.1002/anie.201507140
Guidance literature:
at 210 ℃;
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