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Diflumidone

Base Information
  • Chemical Name:Diflumidone
  • CAS No.:22736-85-2
  • Molecular Formula:C14H11 F2 N O3 S
  • Molecular Weight:311.309
  • Hs Code.:2935009090
  • UNII:E96467495S
  • DSSTox Substance ID:DTXSID90177275
  • Nikkaji Number:J11.481B
  • Wikidata:Q27277039
  • NCI Thesaurus Code:C65384
  • ChEMBL ID:CHEMBL2110671
  • Mol file:22736-85-2.mol
Diflumidone

Synonyms:3-benzoyldifluoromethanesulfonanilide sodium;diflumidone;diflumidone sodium;diflumidone sodium salt;MBR 4164-8;R-807

Suppliers and Price of Diflumidone
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
  • American Custom Chemicals Corporation
  • DIFLUMIDONE 95.00%
  • 5MG
  • $ 503.05
Total 6 raw suppliers
Chemical Property of Diflumidone
Chemical Property:
  • Vapor Pressure:6.7E-08mmHg at 25°C 
  • Boiling Point:438.8°Cat760mmHg 
  • PKA:5.26±0.50(Predicted) 
  • Flash Point:219.2°C 
  • PSA:71.62000 
  • Density:1.419g/cm3 
  • LogP:4.03570 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:5
  • Exact Mass:311.04277071
  • Heavy Atom Count:21
  • Complexity:455
Purity/Quality:

99% *data from raw suppliers

DIFLUMIDONE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(=O)C2=CC(=CC=C2)NS(=O)(=O)C(F)F
  • Uses Diflumidone, is a novel non-steroidal antiinflammatory drug.
Technology Process of Diflumidone

There total 3 articles about Diflumidone 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 sodium hydroxide; In tetrahydrofuran; water; at 25 ℃; for 15h;
DOI:10.1002/anie.201607231
Guidance literature:
Multi-step reaction with 2 steps
1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 h / 0 - 20 °C
2: sodium hydroxide / tetrahydrofuran; water / 15 h / 25 °C
With 3-chloro-benzenecarboperoxoic acid; sodium hydroxide; In tetrahydrofuran; dichloromethane; water;
DOI:10.1002/anie.201607231
Guidance literature:
entspr. NH-Verb., NaOH;
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