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PHENYL ACRIDINE-9-CARBOXYLATE

Base Information Edit
  • Chemical Name:PHENYL ACRIDINE-9-CARBOXYLATE
  • CAS No.:109392-90-7
  • Molecular Formula:C20H13 N O2
  • Molecular Weight:299.329
  • Hs Code.:2933990090
  • Mol file:109392-90-7.mol
PHENYL ACRIDINE-9-CARBOXYLATE

Synonyms:Phenyl9-acridinecarboxylate

Suppliers and Price of PHENYL ACRIDINE-9-CARBOXYLATE
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
  • Ambeed
  • Phenylacridine-9-carboxylate 95+%
  • 5g
  • $ 390.00
  • Ambeed
  • Phenylacridine-9-carboxylate 95+%
  • 1g
  • $ 115.00
  • Ambeed
  • Phenylacridine-9-carboxylate 95+%
  • 250mg
  • $ 45.00
  • Ambeed
  • Phenylacridine-9-carboxylate 95+%
  • 100mg
  • $ 27.00
Total 15 raw suppliers
Chemical Property of PHENYL ACRIDINE-9-CARBOXYLATE Edit
Chemical Property:
  • Vapor Pressure:1.7E-10mmHg at 25°C 
  • Melting Point:188-192 °C  
  • Refractive Index:1.5180 (estimate) 
  • Boiling Point:509.4°Cat760mmHg 
  • PKA:2.63±0.10(Predicted) 
  • Flash Point:261.9°C 
  • PSA:39.19000 
  • Density:1.277g/cm3 
  • LogP:4.60720 
  • Storage Temp.:Sealed in dry,Room Temperature 
Purity/Quality:

98%,99%, *data from raw suppliers

Phenylacridine-9-carboxylate 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 37/39-26 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of PHENYL ACRIDINE-9-CARBOXYLATE

There total 4 articles about PHENYL ACRIDINE-9-CARBOXYLATE 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 potassium tert-butylate; In tetrahydrofuran; for 18h;
DOI:10.1021/ja00251a024
Guidance literature:
With dmap; In dichloromethane; at 20 ℃;
DOI:10.1016/j.saa.2007.10.045
Guidance literature:
Multi-step reaction with 2 steps
1: 87 percent / thionyl chloride / 6 h / Heating
2: 80 percent / potassium tert-butoxide / tetrahydrofuran / 18 h
With thionyl chloride; potassium tert-butylate; In tetrahydrofuran;
DOI:10.1021/ja00251a024
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