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1-(tert-Butylsulfanyl)-4-fluorobenzene

Base Information
  • Chemical Name:1-(tert-Butylsulfanyl)-4-fluorobenzene
  • CAS No.:52323-92-9
  • Molecular Formula:C10H13FS
  • Molecular Weight:184.278
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60495791
  • Nikkaji Number:J1.190.972H
  • Mol file:52323-92-9.mol
1-(tert-Butylsulfanyl)-4-fluorobenzene

Synonyms:52323-92-9;1-(tert-Butylsulfanyl)-4-fluorobenzene;1-tert-butylsulfanyl-4-fluorobenzene;t-butyl 4-fluorophenyl sulfide;SCHEMBL7937564;DTXSID60495791

Suppliers and Price of 1-(tert-Butylsulfanyl)-4-fluorobenzene
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1-(tert-Butylsulfanyl)-4-fluorobenzene
Chemical Property:
  • Vapor Pressure:0.096mmHg at 25°C 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:184.07219975
  • Heavy Atom Count:12
  • Complexity:131
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)SC1=CC=C(C=C1)F
Technology Process of 1-(tert-Butylsulfanyl)-4-fluorobenzene

There total 7 articles about 1-(tert-Butylsulfanyl)-4-fluorobenzene 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 copper(II) bis(trifluoromethanesulfonate); In 1,2-dichloro-ethane; at 40 ℃; for 12h; Sealed tube; Schlenk technique;
DOI:10.1021/acs.orglett.0c04206
Guidance literature:
4-(isopropylthio)-1-fluorobenzene; With n-butyllithium; In tetrahydrofuran; hexane; at -85 ℃; for 6h;
methyl iodide; In tetrahydrofuran; hexane; at 20 ℃; for 3h; Title compound not separated from byproducts;
DOI:10.1016/S0022-1139(99)00097-4
Guidance literature:
With [(C6H3(OP(i-Pr)2)2)RhHCl]; sodium t-butanolate; In toluene; at 110 ℃; for 24h; Sealed tube; Inert atmosphere;
DOI:10.1021/ja505576g
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