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Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]-

Base Information Edit
  • Chemical Name:Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]-
  • CAS No.:62220-57-9
  • Molecular Formula:C16H19NOS
  • Molecular Weight:273.399
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80356597
  • Wikidata:Q82136039
  • Mol file:62220-57-9.mol
Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]-

Synonyms:62220-57-9;Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]-;SCHEMBL11632956;DTXSID80356597;AKOS005066509

Suppliers and Price of Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]-
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
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Total 0 raw suppliers
Chemical Property of Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]- Edit
Chemical Property:
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:273.11873540
  • Heavy Atom Count:19
  • Complexity:259
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CN(C)CC1=CC=CC=C1SC2=CC=CC=C2CO
Technology Process of Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]-

There total 9 articles about Benzenemethanol, 2-[[2-[(dimethylamino)methyl]phenyl]thio]- 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 6 steps
1: thionyl chloride / 5 h / 60 °C
2: 0.5 h / Heating
3: 37 percent / KOH / ethanol / 96 h / Ambient temperature
4: 20.1 g / thionyl chloride
5: 27.0 g / dioxane; H2O / 1 h
6: LiAlH4 / tetrahydrofuran / Ambient temperature
With potassium hydroxide; lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; 1,4-dioxane; ethanol; water;
DOI:10.1021/jo00321a020
Guidance literature:
Multi-step reaction with 3 steps
1: 20.1 g / thionyl chloride
2: 27.0 g / dioxane; H2O / 1 h
3: LiAlH4 / tetrahydrofuran / Ambient temperature
With lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; 1,4-dioxane; water;
DOI:10.1021/jo00321a020
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