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2,5-DIMETHYLTHIOANISOLE

Base Information
  • Chemical Name:2,5-DIMETHYLTHIOANISOLE
  • CAS No.:66623-67-4
  • Molecular Formula:C9H12S
  • Molecular Weight:152.25700
  • Hs Code.:2930909090
2,5-DIMETHYLTHIOANISOLE

Synonyms:2,3',5-trimethyldiphenylmethane;2,3',5-Trimethyl-diphenylmethan;<2,5-Dimethyl-phenyl>-methyl-sulfid;2,5-dimethylthioanisole;

Suppliers and Price of 2,5-DIMETHYLTHIOANISOLE
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
  • Crysdot
  • (2,5-Dimethylphenyl)(methyl)sulfane 97%
  • 100g
  • $ 518.00
  • American Custom Chemicals Corporation
  • 2,5-DIMETHYLTHIOANISOLE 95.00%
  • 5MG
  • $ 505.43
  • AHH
  • 2,5-DIMETHYLTHIOANISOLE 97%
  • 5g
  • $ 100.00
Total 5 raw suppliers
Chemical Property of 2,5-DIMETHYLTHIOANISOLE
Chemical Property:
  • Boiling Point:226-228 °C 
  • PSA:25.30000 
  • Density:1.004 g/cm3(Temp: 30 °C) 
  • LogP:3.02530 
Purity/Quality:

99% *data from raw suppliers

(2,5-Dimethylphenyl)(methyl)sulfane 97% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2,5-DIMETHYLTHIOANISOLE

There total 5 articles about 2,5-DIMETHYLTHIOANISOLE 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 pyridine; CoCl2; In acetonitrile; for 0.25h; Irradiation;
DOI:10.1039/c39940001993
Guidance literature:
With tert-butylammonium hexafluorophosphate(V); platinum; In liquid sulphur dioxide; at -15 ℃; for 3h; Electrochemical reaction;
DOI:10.1016/S0040-4039(99)01311-8
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