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Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)-

Base Information
  • Chemical Name:Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)-
  • CAS No.:79332-47-1
  • Molecular Formula:C14H10Cl2O2S
  • Molecular Weight:313.204
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00356579
  • Wikidata:Q82135998
Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)-

Synonyms:Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)-;79332-47-1;DTXSID00356579

Suppliers and Price of Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)-
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
Total 1 raw suppliers
Chemical Property of Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)-
Chemical Property:
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:311.9778561
  • Heavy Atom Count:19
  • Complexity:308
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)SC2=C(C=C(C=C2Cl)Cl)CC(=O)O
Technology Process of Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)-

There total 7 articles about Benzeneacetic acid, 3,5-dichloro-2-(phenylthio)- 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 hydroxide; In ethanol; water; for 3h; Heating;
DOI:10.1135/cccc19810781
Guidance literature:
Multi-step reaction with 5 steps
1: 78 percent / K2CO3, CuCl / dimethylformamide / 4 h / 140 °C
2: 87 percent / LiAlH4 / diethyl ether / 2.5 h / Heating
3: 96 percent / SOCl2 / benzene / 1.) 25 deg C, 20 min 2.) 60 deg C, 1 h 3.) reflux 1.5 h
4: 50 percent / dimethylformamide / 2 h / 35 °C
5: 98 percent / KOH / ethanol; H2O / 3 h / Heating
With potassium hydroxide; lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; copper(l) chloride; In diethyl ether; ethanol; water; N,N-dimethyl-formamide; benzene;
DOI:10.1135/cccc19810781
Guidance literature:
Multi-step reaction with 3 steps
1: 96 percent / SOCl2 / benzene / 1.) 25 deg C, 20 min 2.) 60 deg C, 1 h 3.) reflux 1.5 h
2: 50 percent / dimethylformamide / 2 h / 35 °C
3: 98 percent / KOH / ethanol; H2O / 3 h / Heating
With potassium hydroxide; thionyl chloride; In ethanol; water; N,N-dimethyl-formamide; benzene;
DOI:10.1135/cccc19810781
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