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Technology Process of Dinsed

Dinsed

Base Information
  • Chemical Name:Dinsed
  • CAS No.:96-62-8
  • Molecular Formula:C14H14N4O8S2
  • Molecular Weight:430.419
  • Hs Code.:2935009090
  • NSC Number:5109
  • UNII:P4KIO8KEG5
  • DSSTox Substance ID:DTXSID3046297
  • Nikkaji Number:J4.721J
  • Wikidata:Q27286152
  • NCI Thesaurus Code:C174832
  • ChEMBL ID:CHEMBL2104289
  • Mol file:96-62-8.mol
Dinsed

Synonyms:dinitrodiphenylsulfonylethylenediamine;dinsed

Suppliers and Price of Dinsed
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
  • Dinsed
  • 25mg
  • $ 75.00
  • American Custom Chemicals Corporation
  • DINSED 95.00%
  • 5MG
  • $ 504.99
Total 10 raw suppliers
Chemical Property of Dinsed
Chemical Property:
  • Vapor Pressure:2.75E-17mmHg at 25°C 
  • Melting Point:189-191° (some decompn) 
  • Boiling Point:659.9°Cat760mmHg 
  • PKA:9.05±0.50(Predicted) 
  • Flash Point:352.9°C 
  • PSA：200.74000 
  • Density:1.563g/cm3 
  • LogP:4.74960 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:7
  • Exact Mass:430.02530576
  • Heavy Atom Count:28
  • Complexity:697
Purity/Quality:

99% *data from raw suppliers

Dinsed *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CC(=C1)S(=O)(=O)NCCNS(=O)(=O)C2=CC=CC(=C2)[N+](=O)[O-])[N+](=O)[O-]
  • Uses Dinsed is a coccidiostat used in poultry to limit/stop the growth of coccidian parasites.
Technology Process of Dinsed

There total 1 articles about Dinsed 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:

N.N'-Bis-<3-nitro-benzolsulfonyl>-aethylendiamin
96-62-8

N.N'-Bis-<3-nitro-benzolsulfonyl>-aethylendiamin

Guidance literature:
aus 3-Nitro-benzolsulfochlorid in Bzl. u. Aethylendiamin in Bzl.<40-60grad>;
Refernces

A Newly Designed Carbohydrate-Derived Alkylamine Promotes Ullmann Type C-N Coupling Catalyzed by Copper in Water

10.1055/s-0037-1611695

The research aimed to develop a green and biodegradable carbohydrate-derived alkylamine ligand for copper-catalyzed Ullmann type C–N coupling reactions in water, offering an environmentally friendly alternative to traditional organic solvents. The study successfully demonstrated that this ligand could promote the coupling of aryl iodides and N-nucleophiles, yielding moderate to excellent results. The methodology was found to be environmentally friendly and economical due to the use of aqueous media instead of organic solvents. The research concluded that the carbohydrate-derived alkylamine not only chelated copper but also enhanced the solubility of 4-iodoanisole in water, making the Ullmann C–N coupling more efficient in an aqueous environment.

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Total 8 Pictures about this product