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Chemical Structure| 7726-20-7 Chemical Structure| 7726-20-7

Structure of 7726-20-7

Chemical Structure| 7726-20-7

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Product Details of [ 7726-20-7 ]

CAS No. :7726-20-7
Formula : C16H34O2S
M.W : 290.51
SMILES Code : O=S(CCCCCCCC)(CCCCCCCC)=O
MDL No. :MFCD00039760

Safety of [ 7726-20-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 7726-20-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 7726-20-7 ]

[ 7726-20-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1986-89-6 ]
  • [ 7726-20-7 ]
  • 2
  • [ 2690-08-6 ]
  • [ 7726-20-7 ]
  • [ 1986-89-6 ]
YieldReaction ConditionsOperation in experiment
37% With dihydrogen peroxide; In water; at 50.0℃; for 4.0h; General procedure: A test tube equipped with a magnetic stirring bar was charged with thioanisole (130.3 mg, 1.0 mmol), aqueous 35% H2O2 (247.7 mg, 2.5 mmol), and Ti-IEZ-MWW (9.9 mg). The mixture was stirred at 50C for 3 h. The conversion and yield were determined by GC analysis of the toluene solution with biphenyl as an internal standard. The yield of methyl phenyl sulfone was>99%, conversion of thioanisole was >99%, and selectivity (yield/conversion) was >99%.
With dihydrogen peroxide; In water; at 25.0℃; for 4.0h;Green chemistry; General procedure: A test tube equipped with a magnetic stirring bar was charged with thioanisole (1.24 g, 10.0 mmol), aqueous 30% H2O2(1.13 g, 9.9 mmol), and Ti-IEZ-MWW (100.2 mg). The mixture was vigorously stirred at 25 C for 2 h. The organic phase was separated, and the organic phase was washed with saturated aqueous Na2S2O3 (10 mL). The organic phase was purified by column chromatography on silica gel using 5:1 hexane / ethylacetate as an eluent to give methyl phenyl sulfoxide as colorless crystals; yield: 0.95 g (70%).
With 1H-imidazole; [(2-(2'-hydroxyphenyl)-5,6-dihydro-1,3-oxazine)2Mn(OAc)]; urea hydrogen peroxide adduct; In methanol; dichloromethane; at 20.0℃; for 0.08333330000000001h; General procedure: To a solution of sulfide (0.2 mmol), imidazole(ImH) (0.2 mmol) as axial ligand, chlorobenzene (0.2mmol) as internal standard, and [(N-O)2Mn(OAc)] (0.01 mmol) in a 1 : 1 mixture of CH3OH/CH2Cl2 (1 mL) was added 0.4 mmol UHP as oxidant. The mixture was stirred at room temperature and the reaction progress monitored by GC. Assignments of products were made by comparison with authentic samples.
With dihydrogen peroxide; In water; at 25.0℃; for 4.0h; General procedure: A test tube equipped with a magnetic stirring bar was charged with thioanisole (1.24 g, 10.0 mmol), aqueous 35% H2O2 (1.16 g, 12.0 mmol), and Ti-IEZ-MWW (100.2 mg). The mixture was vigorously stirred at 25C for 2 h. The organic phase was separated and then washed with saturated aqueous Na2S2O3(10 ml). The organic phase was purified by column chromatography on silica gel using 5:1 hexane/ethyl acetate as an eluent to give methyl phenyl sulfoxide as colorless crystals; yield: 1.33 g (83%).

 

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