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3,5-DICHLOROBISPHENOLA

Base Information
  • Chemical Name:3,5-DICHLOROBISPHENOLA
  • CAS No.:14151-65-6
  • Molecular Formula:C15H14Cl2O2
  • Molecular Weight:297.181
  • Hs Code.:
  • Mol file:14151-65-6.mol
3,5-DICHLOROBISPHENOLA

Synonyms:2-(3,5-dichloro-4-hydroxyphenyl)-2-(4-hydroxyphenyl)propane;2,6-dichlorobisphenol A;Phenol,2,6-dichloro-4-[1-(4-hydroxyphenyl)-1-methylethyl];

Suppliers and Price of 3,5-DICHLOROBISPHENOLA
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
  • 3,5-DichlorobisphenolA
  • 100mg
  • $ 1455.00
  • Medical Isotopes, Inc.
  • 3,5-DichlorobisphenolA
  • 100 mg
  • $ 2200.00
Total 3 raw suppliers
Chemical Property of 3,5-DICHLOROBISPHENOLA
Chemical Property:
  • Melting Point:100-101 °C(Solv: cyclohexane (110-82-7)) 
  • Boiling Point:399.0±37.0 °C(Predicted) 
  • PKA:8.98±0.10(Predicted) 
  • PSA:40.46000 
  • Density:1.329±0.06 g/cm3(Predicted) 
  • LogP:4.73050 
  • Storage Temp.:Room Temperature 
  • Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly) 
Purity/Quality:

99% *data from raw suppliers

3,5-DichlorobisphenolA *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 3,5-Dichlorobisphenol A is an chlorinated derivative of Bisphenol A (B519495), a monomer used for policarbonate and epoxy resins; exhibits estrogenic activity.
Technology Process of 3,5-DICHLOROBISPHENOLA

There total 4 articles about 3,5-DICHLOROBISPHENOLA 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:
Multi-step reaction with 3 steps
1: 90 percent / triethylamine / CH2Cl2 / 15 h / 20 °C
2: 34 percent / sodium hypochlorite / methanol / 1 h
3: 55 percent / K2CO3 / methanol / 2 h / 20 °C
With sodium hypochlorite; potassium carbonate; triethylamine; In methanol; dichloromethane;
DOI:10.1016/S0045-6535(00)00507-5
Guidance literature:
Multi-step reaction with 2 steps
1: 34 percent / sodium hypochlorite / methanol / 1 h
2: 55 percent / K2CO3 / methanol / 2 h / 20 °C
With sodium hypochlorite; potassium carbonate; In methanol;
DOI:10.1016/S0045-6535(00)00507-5
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