Conditions | Yield |
---|---|
With sodium periodate; ruthenium-carbon composite In water at 20℃; for 2h; | 100% |
With C4H9N2O9W In methanol; water at 20℃; for 1.16h; chemoselective reaction; | 99% |
With anthracene; oxygen; acetic acid In isopropyl alcohol at 75℃; for 2h; Temperature; Irradiation; | 99% |
Conditions | Yield |
---|---|
With sodium molybdate dihydrate; dihydrogen peroxide In methanol; water at 25℃; for 0.5h; Kinetics; Concentration; | 100% |
With iron(II) perchlorate monohydrate; ozone; acetonitrile | 100% |
With dihydrogen peroxide; [(η5-C5Me5)Mo(CO)3Cl] In acetonitrile at 35℃; for 2h; | 99% |
Conditions | Yield |
---|---|
With ammonium chloride In tetrahydrofuran at -78℃; for 0.25h; | A 97% B n/a |
Conditions | Yield |
---|---|
With ammonium chloride In tetrahydrofuran at 0℃; | A n/a B 96% |
3-(4-chlorophenyl)-4-dimethylsulfiliminofurazan
A
dimethylsulfone
B
3-(4-chlorophenyl)-4-nitrofurazan
Conditions | Yield |
---|---|
With trifluoroacetyl peroxide In dichloromethane Heating; | A n/a B 96% |
Conditions | Yield |
---|---|
With ammonium chloride In tetrahydrofuran at 0℃; | A n/a B 95% |
3-(4-chlorophenyl)-4-dimethylsulfiliminofurazan
A
dimethylsulfone
B
3-(4-chlorophenyl)-4-nitrofurazan
D
azoxy(4-chlorophenylfurazan)
Conditions | Yield |
---|---|
With 4 A molecular sieve; 3,3-dimethyldioxirane In acetone for 16h; Ambient temperature; | A n/a B n/a C 87% D n/a |
Conditions | Yield |
---|---|
In benzene at 20℃; for 6h; | A n/a B 82% |
Conditions | Yield |
---|---|
With oxygen; dimethyl sulfoxide at -40℃; Irradiation; methylene blue sensitizer; | A 79% B n/a |
dimethylsulfide
A
dimethylsulfone
B
((methyl-d3)sulfonyl)methane-d3
C
dimethyl sulfoxide
Conditions | Yield |
---|---|
With <18O,2H6>DMSO; oxygen; methylene blue In [D3]acetonitrile for 0.166667h; Mechanism; Product distribution; Irradiation; | A 7.4% B n/a C 77.5% |
Conditions | Yield |
---|---|
With pinanyl hydroperoxide In various solvent(s) at 80℃; for 70h; | A 71.7% B 75.9% |
Conditions | Yield |
---|---|
for 5h; Product distribution; | A 73% B n/a |
A
dimethylsulfone
B
1-Oxaspiro<4.5>decan-2,3,4-trion
C
dimethyl sulfoxide
Conditions | Yield |
---|---|
With ozone In dichloromethane at 0℃; | A n/a B 73% C n/a |
dimethyl sulfoxide
diazodiphenylmethane
A
benzophenone
B
dimethylsulfone
Conditions | Yield |
---|---|
With oxygen In acetonitrile at 25℃; Product distribution; Flash photolysis; | A 71% B 23.6% |
C8H9ClO2S
benzaldehyde
A
dimethylsulfone
B
(E)-methyl styryl sulfone
C
2-(p-Chlorophenoxy)-2-phenylethyl methyl sulfone
D
2-(Benzoyloxy)-2-phenylethyl methyl sulfone
E
4-chloro-phenol
Conditions | Yield |
---|---|
for 3h; Product distribution; | A 30% B 6% C 4.5% D 6.6% E 70% |
3-chloro-2H-thiete 1,1-dioxide
dimethylsulfone
Conditions | Yield |
---|---|
With sodium hydroxide for 0.166667h; Heating; | 68% |
Bis-[2,6-bis-(difluoro-nitro-methyl)-2,6-bis-trifluoromethyl-3,6-dihydro-2H-[1,3,5]oxadiazin-4-yl]-amine; compound with methanesulfinylmethane
A
dimethylsulfide
B
dimethylsulfone
C
4,4'-iminobis<2,6-bis(difluoronitromethyl)-5,6-dihydro-2,6-bis(trifluoromethyl)-2H-1,3,5-oxadiazine>
Conditions | Yield |
---|---|
With sulfuric acid at 50 - 60℃; for 2h; | A n/a B n/a C 67% |
6-amino-1,3-dimethyl-5-<(p-nitrobenzylidene)amino>uracil
A
8-(p-Nitrophenyl)theophylline
B
dimethylsulfone
Conditions | Yield |
---|---|
With Ni-PO In dimethyl sulfoxide at 80℃; for 7.5h; | A 65% B n/a |
C8H9ClO2S
benzaldehyde
A
dimethylsulfone
B
(E)-methyl styryl sulfone
C
2-(p-Chlorophenoxy)-2-phenylethyl methyl sulfone
D
4-chloro-phenol
Conditions | Yield |
---|---|
at -60℃; for 3h; Product distribution; | A 65% B 27.5% C 22% D n/a |
C8H9ClO2S
4-tercbutyl-cyclohexanone
A
dimethylsulfone
B
(4-tert-Butyl-1-cyclohexenyl)methyl methyl sulfone
C
<1-<(Methylsulfonyl)methyl>-1-(p-chlorophenoxy)-4-tert-butyl>cyclohexane
D
4-chloro-phenol
Conditions | Yield |
---|---|
at -60℃; for 3h; Product distribution; | A 64% B 42% C 3.7% D n/a |
Conditions | Yield |
---|---|
In water at 100℃; for 12h; Sealed tube; | 61% |
With water at 110℃; for 12h; Sealed tube; Green chemistry; | 61% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 26h; | 100% |
3-phenyl-1,3,4,5-tetrahydro-benzo[b]azepine-2-thione
dimethylsulfone
2-methylsulfanyl-3-phenyl-4,5-dihydro-3H-benzo[b]azepine
Conditions | Yield |
---|---|
In sodium hydroxide | 99% |
dimethylsulfone
(3S)-3-hydroxydihydrofuran-2(3H)-one
methyl (S)-4-hydroxy-2-methoxybutyrate
Conditions | Yield |
---|---|
Stage #1: (3S)-3-hydroxydihydrofuran-2(3H)-one With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; Stage #2: dimethylsulfone In tetrahydrofuran at 20℃; Stage #3: potassium carbonate In methanol at 0℃; for 1h; | 99% |
5-bromo-2-fluoro-4-methyl-pyridine
dimethylsulfone
Conditions | Yield |
---|---|
With sodium hexamethyldisilazane In tetrahydrofuran at -30 - 30℃; | 98% |
dimethylsulfone
desoxydemethylenechicanine
isoguaiacin dimethyl ether
Conditions | Yield |
---|---|
With potassium carbonate In acetone | 95% |
dimethylsulfone
3-ethoxy-4-methoxybenzoic acid methyl ester
1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethan-1-one
Conditions | Yield |
---|---|
Stage #1: dimethylsulfone With sodium hydride In hexane at 15 - 35℃; Inert atmosphere; Stage #2: 3-ethoxy-4-methoxybenzoic acid methyl ester In hexane at 30 - 35℃; for 6h; Solvent; Temperature; Reagent/catalyst; Inert atmosphere; | 95% |
With potassium tert-butylate In dimethyl sulfoxide at 55℃; for 1.5h; Temperature; Inert atmosphere; | 50% |
dimethylsulfone
3-Methyl-2-(methylpropionylamino)benzofuran-5-ol
5-Methoxy-3-methyl-2-(methylpropionylamino)benzofuran
Conditions | Yield |
---|---|
With potassium hydroxide In 1,4-dioxane; water Ambient temperature; | 94% |
Conditions | Yield |
---|---|
With platinum on carbon; potassium tert-butylate; hydrogen In toluene under 1875.19 Torr; for 15h; Inert atmosphere; Reflux; | 94% |
With C24H20ClN2OPRu; potassium tert-butylate In 1,4-dioxane at 125℃; for 5h; Inert atmosphere; Schlenk technique; Glovebox; | 50% |
Conditions | Yield |
---|---|
With platinum on carbon; potassium tert-butylate; hydrogen In toluene under 1875.19 Torr; for 12h; Catalytic behavior; Inert atmosphere; Reflux; | 94% |
dimethylsulfone
2,7-dichloro-3,8-dihydroxy-1,4,9-trimethyl-11-oxo-11H-dibenzo<1,4>dioxepin-6-carbaldehyde
2,7-dichloro-3,8-dimethoxy-1,4,9-trimethyl-11-oxo-11H-dibenzo<1,4>dioxepin-6-carbaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 0.25h; Heating; | 93% |
dimethylsulfone
Conditions | Yield |
---|---|
Stage #1: dimethylsulfone With n-butyllithium In tetrahydrofuran; hexane for 0.25h; Metallation; Stage #2: C30H44N2O3S In tetrahydrofuran; hexane for 16h; Substitution; | 93% |
dimethylsulfone
3α,5-cyclo-23,24-dinor-6β-methoxy-5α-cholane-24-al (E)-tosylhydrazone
6β-methoxy-3α,5-cyclo-24-nor-5α-chol-22-ene
Conditions | Yield |
---|---|
Stage #1: dimethylsulfone With n-butyllithium In tetrahydrofuran; hexane for 0.25h; Stage #2: 3α,5-cyclo-23,24-dinor-6β-methoxy-5α-cholane-24-al (E)-tosylhydrazone In tetrahydrofuran; hexane at 20℃; for 16h; Further stages.; | 93% |
dimethylsulfone
3-ethoxy-4-methoxybenzenecarbonitrile
1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethan-1-one
Conditions | Yield |
---|---|
Stage #1: dimethylsulfone With n-butyllithium In tetrahydrofuran; hexane Large scale; Stage #2: 3-ethoxy-4-methoxybenzenecarbonitrile In tetrahydrofuran; hexane at 0 - 5℃; Large scale; Stage #3: With hydrogenchloride; water In tetrahydrofuran; hexane Large scale; | 93% |
Stage #1: dimethylsulfone With n-butyllithium In tetrahydrofuran; hexane at 0 - 10℃; for 3h; Inert atmosphere; Stage #2: 3-ethoxy-4-methoxybenzenecarbonitrile In tetrahydrofuran at 0 - 20℃; for 6h; | 81% |
Stage #1: dimethylsulfone With n-butyllithium In tetrahydrofuran; hexane at 0 - 10℃; for 3h; Inert atmosphere; Industrial scale; Stage #2: 3-ethoxy-4-methoxybenzenecarbonitrile In tetrahydrofuran at 0 - 20℃; for 6h; Solvent; Concentration; Industrial scale; | 81% |
Conditions | Yield |
---|---|
at 85 - 90℃; for 312h; sealed flask; | 92% |
dimethylsulfone
3-ethoxy-4-methoxybenzaldehyde
2-(3-ethoxy-4-methoxyphenyl)-1-(methylsulfonyl)eth-2-ylamine
Conditions | Yield |
---|---|
Stage #1: dimethylsulfone With n-butyllithium In tetrahydrofuran; hexane at -20 - 0℃; for 1h; Stage #2: 3-ethoxy-4-methoxybenzaldehyde With lithium hexamethyldisilazane In tetrahydrofuran; hexane at -40 - -30℃; for 1h; Stage #3: With boron trifluoride diethyl etherate In tetrahydrofuran; hexane at -30 - 0℃; Temperature; | 91.5% |
Stage #1: 3-ethoxy-4-methoxybenzaldehyde With lithium hexamethyldisilazane at -78℃; Stage #2: dimethylsulfone With n-butyllithium; boron trifluoride diethyl etherate at -78℃; | 41% |
dimethylsulfone
2-phenyl-4,5-tridecamethylenepyrazolone
2-phenyl-1-methyl-4,5-tridecamethylenepyrazol-3-one
Conditions | Yield |
---|---|
In toluene at 120℃; for 1.5h; | 91% |
Product Name: Methyl sulfone (CAS NO.67-71-0)
IUPAC Name: methylsulfonylmethane
Molecular Formula: C2H6O2S
Molecular Weight: 94.132840 g/mol
Appearance: white crystalline flakes, great Stink
Density:1,16 g/cm3
Melting Point: 108-110 °C
Boiling Point: 238 °C
Flash Point: 143 °C
Solubility: water, ethanol, benzene, methanol and acetone, slightly soluble in ether and chloroform
Water Solubility: 150 g/L (20 °C)
Merck: 14,3258
BRN: 1737717
Index of Refraction: 1.402
Molar Refractivity: 20.11 cm3
Molar Volume: 82.5 cm3
Categories: Pharmaceutical Intermediates; Miscellaneous; Nutritional Supplements; Food & Flavor Additives
Methyl sulfone (CAS NO.67-71-0) is used as a high temp solvent for many inorganic and organic substances. It is also used as gas chromatography stationary phase and analytical reagent.
Safety Information of Methyl sulfone (CAS NO.67-71-0):
Safety Statements:22-24/25
22:Do not breathe dust
24/25:Avoid contact with skin and eyes
WGK Germany:1
RTECS:PB2785000
HS Code:29309070
Methyl sulfone , its CAS NO. is 67-71-0, the synonyms are Dimethyl sulfone ; Dimethyl sulphone ; MSM ; Methyl sulfone ; Methylsulfonylmethane ; Sulfonylbismethane ; Dimethyl sulphone ; Methane, 1,1'-sulfonylbis- ; Methane, sulfonylbis- ; Methyl sulfone ; Methane, sulfonylbis- ; Methylsulfonyl methane ; Sulfonylbismethane .
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