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2-Phenoxybenzenethiol

Base Information Edit
  • Chemical Name:2-Phenoxybenzenethiol
  • CAS No.:55710-19-5
  • Molecular Formula:C12H10OS
  • Molecular Weight:202.277
  • Hs Code.:
  • DSSTox Substance ID:DTXSID00444344
  • Nikkaji Number:J1.748.089H
  • Wikidata:Q82262463
  • Mol file:55710-19-5.mol
2-Phenoxybenzenethiol

Synonyms:2-phenoxybenzenethiol;55710-19-5;Benzenethiol, 2-phenoxy-;2-phenoxybenzene-1-thiol;SCHEMBL1930320;DTXSID00444344;CS-0355959;EN300-1863955

Suppliers and Price of 2-Phenoxybenzenethiol
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
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of 2-Phenoxybenzenethiol Edit
Chemical Property:
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:202.04523611
  • Heavy Atom Count:14
  • Complexity:166
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)OC2=CC=CC=C2S
Technology Process of 2-Phenoxybenzenethiol

There total 7 articles about 2-Phenoxybenzenethiol 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 sulfur; In diethyl ether; at 0 ℃; for 0.5h; Inert atmosphere;
Guidance literature:
phenoxathiine; With lithium; In tetrahydrofuran; at -78 ℃; for 0.75h;
With water; at -78 ℃; for 0.25h;
DOI:10.1246/cl.2002.726
Guidance literature:
diphenylether; With trifluoromethylsulfonic anhydride; (MeO2CH2CH2)2SO; In dichloromethane; at -35 - 20 ℃;
With triethylamine; In tetrahydrofuran; at 20 ℃; for 12h;
With potassium tert-butylate; In tetrahydrofuran; at -78 ℃; for 0.166667h; Title compound not separated from byproducts;
DOI:10.1021/jo034013h
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