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Pyridarone

Base Information Edit
  • Chemical Name:Pyridarone
  • CAS No.:7035-04-3
  • Molecular Formula:C13H9 N O
  • Molecular Weight:0
  • Hs Code.:2934999090
  • NSC Number:85430
  • UNII:83L91231V7
  • DSSTox Substance ID:DTXSID50220630
  • Nikkaji Number:J2.373.356K
  • Wikidata:Q27116027
  • NCI Thesaurus Code:C72591
  • Metabolomics Workbench ID:54973
  • ChEMBL ID:CHEMBL2105396
  • Mol file:7035-04-3.mol
Pyridarone

Synonyms:4-(2-benzofuranyl)pyridine

Suppliers and Price of Pyridarone
Supply Marketing:Edit
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
  • 4-(1-BENZOFURAN-2-YL)PYRIDINE 95.00%
  • 5G
  • $ 1168.42
  • American Custom Chemicals Corporation
  • 4-(1-BENZOFURAN-2-YL)PYRIDINE 95.00%
  • 2.5G
  • $ 983.88
  • American Custom Chemicals Corporation
  • 4-(1-BENZOFURAN-2-YL)PYRIDINE 95.00%
  • 1G
  • $ 721.57
Total 4 raw suppliers
Chemical Property of Pyridarone Edit
Chemical Property:
  • Vapor Pressure:0.000267mmHg at 25°C 
  • Boiling Point:333.3°C at 760 mmHg 
  • Flash Point:155.3°C 
  • PSA:26.03000 
  • Density:1.184g/cm3 
  • LogP:3.49480 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:195.068413911
  • Heavy Atom Count:15
  • Complexity:213
Purity/Quality:

95% *data from raw suppliers

4-(1-BENZOFURAN-2-YL)PYRIDINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=C(O2)C3=CC=NC=C3
Technology Process of Pyridarone

There total 9 articles about Pyridarone 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 trifluorormethanesulfonic acid; In 1,4-dioxane; at 120 ℃; for 12h;
DOI:10.1039/c3ob42039f
Guidance literature:
4-pyridinecarboxylic acid, methyl ester; ortho-bromophenylacetic acid; With sodium hexamethyldisilazane; In tetrahydrofuran; N,N-dimethyl-formamide; at -10 ℃; for 3.5h; Inert atmosphere;
With potassium dihydrogenphosphate; copper(l) iodide; potassium phosphate tribasic heptahydrate; In tetrahydrofuran; N,N-dimethyl-formamide; at 110 ℃; for 6h; Inert atmosphere;
DOI:10.1039/c2gc16457d
Guidance literature:
Multi-step reaction with 2 steps
1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere
2: trifluorormethanesulfonic acid / 1,4-dioxane / 12 h / 120 °C
With trifluorormethanesulfonic acid; potassium carbonate; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1039/c3ob42039f
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