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CHLOROMETHYL PHENYL SULFOXIDE

  • Product Name CHLOROMETHYL PHENYL SULFOXIDE
  • cas 7205-94-9
  • purity 99%
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High Quality Chinese Manufacturer supply 7205-94-9 CHLOROMETHYL PHENYL SULFOXIDE

  • Molecular Formula: C7H7 Cl O S
  • Molecular Weight: 174.651
  • Vapor Pressure: 0.00125mmHg at 25°C 
  • Melting Point: 33-35 °C
     
  • Boiling Point: 109-111 °C0.01 mm Hg
     
  • Flash Point: 100 °C 
  • PSA: 36.28000 
  • Density: 1.35g/cm3 
  • LogP: 2.85620 

CHLOROMETHYL PHENYL SULFOXIDE(Cas 7205-94-9) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 90, p. 4496, 1968 DOI: 10.1021/ja01018a078Synthesis, p. 831, 1986Tetrahedron Letters, 17, p. 613, 1976

General Description

Chloromethyl phenyl sulfoxide has synthetic potential and exhibits unusual stereochemical specificity. Stereospecific hydroxyalkylation of chloromethyl phenyl sulfoxide has been investigated.

InChI:InChI=1/C7H7ClOS/c8-6-10(9)7-4-2-1-3-5-7/h1-5H,6H2

7205-94-9 Relevant articles

Aldehyde to Ketone Homologation Enabled by Improved Access to Thioalkyl Phosphonium Salts

Fragis, Meghan,Deobald, Jackson L.,Dharavath, Srinivas,Scott, Jeffrey,Magolan, Jakob

supporting information, p. 4548 - 4552 (2021/06/28)

Phosphines were previously unusable as P...

Selectivity switch in the aerobic oxygenation of sulfides photocatalysed by visible-light-responsive decavanadate

Li, Chifeng,Mizuno, Noritaka,Murata, Kei,Ishii, Kazuyuki,Suenobu, Tomoyoshi,Yamaguchi, Kazuya,Suzuki, Kosuke

supporting information, p. 3896 - 3905 (2020/07/09)

Nanometre-sized metal oxides are promisi...

Sulfone compound (by machine translation)

-

Paragraph 0046, (2017/10/06)

[Problem] to safely and conveniently, hi...

Chemoselective Oxidation of Sulfides to Sulfoxides with Urea-Hydrogen Peroxide Complex Catalysed by Diselenide

Bulman Page, Philip C.,Buckley, Benjamin R.,Elliott, Claire,Chan, Yohan,Dreyfus, Nicolas,Marken, Frank

supporting information, p. 80 - 82 (2015/12/26)

A highly selective catalytic oxidation s...

7205-94-9 Process route

phenylthiomethyl chloride
7205-91-6

phenylthiomethyl chloride

chloromethyl phenyl sulfoxide
7205-94-9

chloromethyl phenyl sulfoxide

Conditions
Conditions Yield
With n-C4F9; perfluoro-cis-2,3-dialkyloxaziridine; n-C3F7; In chloroform; trichlorofluoromethane; at -40 ℃; for 0.5h;
95%
With aluminum oxide; sodium chlorite; manganese(III) acetylacetonate; In acetone; at 20 ℃; for 0.5h;
95%
With aluminum oxide; calcium hypochlorite; In dichloromethane; at 30 ℃; for 0.833333h;
91%
With 5,10,15,20-tetrakis(pentafluorophenyl)-21H,23H-porphyrin iron(III) chloride; dihydrogen peroxide; In ethanol; at 20 ℃; for 0.0666667h;
90%
With 1-butyl-4-aza-1-azoniabicyclo[2.2.2]octane dichromate; In acetonitrile; for 1.08333h; Heating;
89%
With nitric acid; phosphorus pentoxide; silica gel; In water; for 0.0833333h;
88%
With nitric acid; phosphorus pentoxide; silica gel; for 0.0833333h;
88%
With nitrourea; silica-gel-supported sulfuric acid; ammonium bromide; In dichloromethane; at 20 ℃; for 2.66667h;
84%
With dihydrogen peroxide; vanadium(III) chloride; In tetrahydrofuran; at 20 ℃; for 0.583333h;
83%
With sulfuryl dichloride; water; silica gel; In dichloromethane; for 2h; Ambient temperature;
80.8%
With iron(III) chloride; periodic acid; In acetonitrile; at 20 ℃; for 0.0833333h;
80%
With N-Bromosuccinimide; In methanol; water; at 0 - 5 ℃;
42%
With dihydrogen peroxide; zinc dibromide; In 1,4-dioxane; water; at 20 ℃; for 6h; Air atmosphere;
60 %Chromat.
With diphenyl diselenide; urea hydrogen peroxide adduct; In dichloromethane; at 20 ℃; for 24h;
96 %Spectr.
methyl-phenyl-thioether
100-68-5

methyl-phenyl-thioether

chloromethyl phenyl sulfoxide
7205-94-9

chloromethyl phenyl sulfoxide

Conditions
Conditions Yield
With sulfuryl dichloride; silver nitrate; In acetonitrile; at 0 - 25 ℃; for 1h;
84%
methyl-phenyl-thioether; With sulfuryl dichloride; In dichloromethane; for 2h; Heating;
With sulfuryl dichloride; water; silica gel; In dichloromethane; at 20 ℃; for 2h;
84%
Multi-step reaction with 2 steps
1: N-chloro-succinimide / chlorobenzene / 3 h / 35 °C / Inert atmosphere
2: N-Bromosuccinimide / water; methanol / 0 - 5 °C
With N-chloro-succinimide; N-Bromosuccinimide; In methanol; water; chlorobenzene;
Multi-step reaction with 2 steps
1: dihydrogen peroxide / water; methanol / 24 h / 0 - 20 °C
2: N-chloro-succinimide / dichloromethane / 48 h / 20 °C
With N-chloro-succinimide; dihydrogen peroxide; In methanol; dichloromethane; water;

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