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5-Chloro-2-phenyl-1,3-indandione

Base Information
  • Chemical Name:5-Chloro-2-phenyl-1,3-indandione
  • CAS No.:1470-36-6
  • Molecular Formula:C15H9 Cl O2
  • Molecular Weight:256.6838
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00933001
5-Chloro-2-phenyl-1,3-indandione

Synonyms:1470-36-6;BRN 2112627;5-Chloro-2-phenyl-1,3-indandione;1,3-Indandione, 5-chloro-2-phenyl-;SCHEMBL14939892;DTXSID00933001;5-Chloro-2-phenyl-1H-indene-1,3(2H)-dione

Suppliers and Price of 5-Chloro-2-phenyl-1,3-indandione
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
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Total 0 raw suppliers
Chemical Property of 5-Chloro-2-phenyl-1,3-indandione
Chemical Property:
  • Vapor Pressure:2.71E-08mmHg at 25°C 
  • Boiling Point:450.1°Cat760mmHg 
  • Flash Point:189.6°C 
  • Density:1.367g/cm3 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:256.0291072
  • Heavy Atom Count:18
  • Complexity:360
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C2C(=O)C3=C(C2=O)C=C(C=C3)Cl
Technology Process of 5-Chloro-2-phenyl-1,3-indandione

There total 3 articles about 5-Chloro-2-phenyl-1,3-indandione 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 acetate; at 220 - 240 ℃; Erwaermen des Reaktionsprodukts mit methanol. Natriummethylat;
Guidance literature:
Multi-step reaction with 2 steps
1.1: 90 percent / acetic anhydride / 1 h / Heating
2.1: Ac2O; Et3N / 1.5 h / Heating
2.2: NaOMe / methanol / 0.75 h
With acetic anhydride; triethylamine;
DOI:10.1016/j.bmcl.2005.11.041
Guidance literature:
With triethylamine; In acetic anhydride; Reflux;
With sodium methylate; In methanol; acetic anhydride; Reflux;
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