Conditions | Yield |
---|---|
Stage #1: dichloromethane With calcium sulfite In water at 180℃; for 10h; Autoclave; Stage #2: calcium methanedisulfonate With sulfuric acid In water at 80℃; for 2h; Reagent/catalyst; Temperature; | 89% |
Conditions | Yield |
---|---|
Stage #1: 1,2-dibromomethane With potassium sulfite; tetrabutylammomium bromide; potassium iodide In water at 80 - 90℃; for 88h; Stage #2: With hydrogenchloride In water at 90℃; for 2h; Stage #3: With barium(II) chloride In water at 20 - 90℃; for 2h; | 84.7% |
methylene trithiocarbonate
methanedisulfonic acid
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With sulfuric acid; sulfur trioxide bis zum Entweichen von schwefliger Saeure; | |
With sulfuric acid; sulfur trioxide at 210℃; |
LACTIC ACID
methanedisulfonic acid
Conditions | Yield |
---|---|
With sulfuric acid; sulfur trioxide bis zur Entwicklung von schwefliger Saeure, dann Saettigen mit BaCO3; | |
With sulfuric acid; sulfur trioxide |
Conditions | Yield |
---|---|
With sulfur trioxide |
Conditions | Yield |
---|---|
With sulfur trioxide at 140℃; | |
With aminosulfonic acid at 25 - 150℃; for 3h; Reagent/catalyst; Temperature; |
Conditions | Yield |
---|---|
With sulfur trioxide |
Conditions | Yield |
---|---|
With potassium sulfite at 150℃; |
dimethyl methanedisulfonate
ethanol
A
diethyl ether
B
methanedisulfonic acid
Conditions | Yield |
---|---|
With potassium sulfite at 180℃; |
Conditions | Yield |
---|---|
With hydrogenchloride; acetic acid bei der elektrolytischen Oxydation; | |
durch Hypochlorite; |
sulfoacetic acid
A
formaldehyd
B
ethane-1,2-disulphonic acid
C
methanedisulfonic acid
Conditions | Yield |
---|---|
bei der elektrolytischen Oxydation von sulfoessigsauren Salzen,und Kochen der angesaeuerten Loesung (Entwicklung von CO2,H2SO4,CO,SO2,Aethylen); |
Conditions | Yield |
---|---|
With sulfuric acid at 75 - 80℃; bei der elektrolytischen Oxydation an PbO2; | |
With water at 75 - 80℃; bei der elektrolytischen Oxydation an Platin; |
Conditions | Yield |
---|---|
With alkali |
disulfoacetic acid
methanedisulfonic acid
Conditions | Yield |
---|---|
durch thermische Zersetzung; |
N-acetyl-N-methylaniline
A
methanedisulfonic acid
B
N-methylorthanilic acid
Conditions | Yield |
---|---|
With sulfuric acid at 140 - 150℃; |
Conditions | Yield |
---|---|
With sulfuric acid; sulfur trioxide at 120℃; durch Zufuegen von Eisessig und weiteres Erhitzen auf 120grad; |
Conditions | Yield |
---|---|
With chlorosulfonic acid unter Kuehlung und Erhitzen des Reaktionsgemisches dann auf 140grad; |
Conditions | Yield |
---|---|
With chlorosulfonic acid unter Kuehlung und Erhitzen des Reaktionsgemisches dann auf 140grad; |
Conditions | Yield |
---|---|
With sulfuric acid; sulfur trioxide | |
With methanol; sulfuric acid; sulfur trioxide |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With sulfuric acid; sulfur trioxide ueber mehrere Stufen; | |
With sulfuric acid |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With sulfuric acid entstehen noch Sulfaten wie HO3SOCH(OH)CH(SO3H)2, welche bei der Spaltung mit Salzsaeure ebenfalls Acetaldehyddisulfonsaeure liefern; |
Conditions | Yield |
---|---|
(hydrolysis); |
methanedisulfonic acid
Conditions | Yield |
---|---|
With piperidine |
methanedisulfonic acid
Conditions | Yield |
---|---|
(i) aq. HCl, BaCl2, (ii) aq. H2SO4; Multistep reaction; |
Conditions | Yield |
---|---|
In water at 20℃; for 6h; | 99% |
Conditions | Yield |
---|---|
In water addn. of Ag2CO3 to an aq. soln. of the sulfonic acid; filtn., evapd. in vac., dried in vac. at 50°C; elem. anal.; | 98% |
In water exclusion of light; filtn., pptn. on evapn., drying (vac., 50°C); elem. anal.; | 98% |
In water (N2); Schlenk technique; aq. soln. of acid was added dropwise into stirred aq. soln. of Ag salt at 20°C; filtered through Celite; stirredat 20°C for 1 h; evapd. (vac.); dried at 50°C in vac.; | 84% |
In water |
methanedisulfonic acid
[(chlorosulfonyl)oxy]methyl sulfurochloridate
methylene methane disulfonate
Conditions | Yield |
---|---|
Stage #1: methanedisulfonic acid With poly(4-vinylpyridine) In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: [(chlorosulfonyl)oxy]methyl sulfurochloridate In 1,2-dichloro-ethane at 55℃; for 5h; Reagent/catalyst; Temperature; | 92% |
Conditions | Yield |
---|---|
With acetic anhydride; phosphorus trichloride at 120℃; for 5h; Reagent/catalyst; Temperature; Time; | 88.72% |
In toluene at 120℃; for 2h; Temperature; Solvent; | 81.2% |
With phosphorus pentoxide In 1,2-dichloro-ethane at 84℃; for 2h; | 76.52% |
With phosphorus pentoxide at 120℃; for 1h; | 47% |
Conditions | Yield |
---|---|
at 120℃; |
Conditions | Yield |
---|---|
at 140℃; man destilliert kontinuerlich der gebildete Aether ueber; | |
at 140℃; |
i-Amyl alcohol
methanedisulfonic acid
A
propan-1-ol
B
2-methyl-but-2-ene
C
isopentyl ether
D
2-methyl-propan-1-ol
Conditions | Yield |
---|---|
With phosphorus pentachloride | |
With phosphorus pentachloride | |
With phosphorus pentachloride |
Molecular Structure of Methanedisulfonic acid (CAS NO.503-40-2):
Molecular Formula: CH4O6S2
Molecular Weight: 176.1689
IUPAC Name: Methanedisulfonic acid
Synonyms of Methanedisulfonic acid (CAS NO.503-40-2): Methionic acid ; EINECS 207-966-4 ; Methanedisulphonic acid
CAS NO: 503-40-2
Index of Refraction: 1.581
Molar Refractivity: 27.37 cm3
Molar Volume: 82.1 cm3
Surface Tension: 119.9 dyne/cm
Density: 2.145 g/cm3
Methanedisulfonic acid (CAS NO.503-40-2) is used as the main additive in the hard chromium plating process.
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