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4-Chlorophenyl methyl sulfoxide, (S)-

Base Information
  • Chemical Name:4-Chlorophenyl methyl sulfoxide, (S)-
  • CAS No.:112456-62-9
  • Molecular Formula:C7H7ClOS
  • Molecular Weight:174.651
  • Hs Code.:
  • UNII:2KC6764B3Z
  • Wikidata:Q27896850
4-Chlorophenyl methyl sulfoxide, (S)-

Synonyms:4-Chlorophenyl methyl sulfoxide, (S)-;2KC6764B3Z;(S)-p-Chlorophenyl methyl sulfoxide;112456-62-9;4-Chlorophenyl methyl sulfoxide, (-)-;1-Chloro-4-((S)-methylsulfinyl)benzene;UNII-2KC6764B3Z;Benzene, 1-chloro-4-((S)-methylsulfinyl)-;SCHEMBL19079696;(S)-4-chlorophenyl methyl sulfoxide;Q27896850

Suppliers and Price of 4-Chlorophenyl methyl sulfoxide, (S)-
Supply Marketing:
Business phase:
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Chemical Property of 4-Chlorophenyl methyl sulfoxide, (S)-
Chemical Property:
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:173.9906137
  • Heavy Atom Count:10
  • Complexity:130
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CS(=O)C1=CC=C(C=C1)Cl
  • Isomeric SMILES:C[S@](=O)C1=CC=C(C=C1)Cl
Technology Process of 4-Chlorophenyl methyl sulfoxide, (S)-

There total 15 articles about 4-Chlorophenyl methyl sulfoxide, (S)- 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 titanium(IV) isopropylate; Cumene hydroperoxide; (R,R)-CH3(CH2)6OOCCH(OH)CH(OH)COO-polyethylene glycol-OMe; In dichloromethane; at -20 ℃; for 16h;
DOI:10.1016/j.tetlet.2007.09.169
Guidance literature:
With C30H34N4O2; dihydrogen peroxide; scandium tris(trifluoromethanesulfonate); In tetrahydrofuran; at -20 ℃; for 0.51h;
Guidance literature:
With MoO(O2)2(H2O); C15H24N2O4; dihydrogen peroxide; tetraphenylphosphonium bromide; In chloroform; water; at 0 ℃; for 1h; enantioselective reaction;
DOI:10.3390/molecules23071595
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