N-sulfonoxy-p-chloroacetanilide pyridinium salt
A
ethyl sulfate
B
N-(4-chlorophenyl)-N-hydroxyacetamide
Conditions | Yield |
---|---|
In ethanol at 40℃; | A 83% B n/a |
In ethanol at 40℃; | A n/a B 83% |
Conditions | Yield |
---|---|
With sodium hydroxide at 150 - 200℃; | |
With ethanol; sodium ethanolate | |
With sodium ethanolate; toluene |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With chlorosulfonic acid |
Conditions | Yield |
---|---|
With sulphur monochloride | |
With chlorosulfonic acid | |
With sulfuric acid |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With sulfuric acid | |
With sulfuric acid; silver | |
With silver salt; sulfuric acid |
Conditions | Yield |
---|---|
With silver hydrogensulfate |
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid In ethanol at -60 - 20℃; |
ethanol
diammonium salt of phenyl phosphatosulfate
A
ethyl sulfate
B
phosphoric acid monophenyl ester
C
ethyl phenyl hydrogen phosphate
Conditions | Yield |
---|---|
With N-ethylmorpholine;; magnesium(II) perchlorate at 55℃; Rate constant; |
chlorobenzene
ethyl ester of p-toluenesulfonic acid
A
ethyl sulfate
B
4-methylphenyl-4-chlorophenyl sulfone
Conditions | Yield |
---|---|
With sulfur trioxide 1.) room temperature, 1h; Multistep reaction; |
ethylnitramine
ethyl sulfate
Conditions | Yield |
---|---|
With sulfuric acid at 25 - 85℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), -ΔS(excit.); |
Conditions | Yield |
---|---|
anschliessend entsteht auch H2SO4; |
chloral ethyl hemiacetal
sulfuric acid
A
ethyl sulfate
B
chloral
Conditions | Yield |
---|---|
Electrolysis; |
1,2-dichloro-2-ethoxyethane
sulfuric acid
A
2-chloroethanal
B
hydrogenchloride
C
ethyl sulfate
Conditions | Yield |
---|---|
at 100℃; bei hoeherer Temp. entsteht Aethylen und schwefliger Saeure; |
ethyl hydroperoxide
sulphurous acid
A
ethyl sulfate
B
sulfuric acid
Conditions | Yield |
---|---|
With sulfuric acid at 25℃; |
2-oxo-1-phenylpropane-1-sulfonic acid
A
ethyl sulfate
B
1-phenyl-acetone
Conditions | Yield |
---|---|
In sulfuric acid; water |
ethanol
sulfur trioxide
A
diethyl sulfate
B
ethyl sulfate
C
2-sulfooxy-ethanesulfonic acid
Conditions | Yield |
---|---|
In liquid sulphur dioxide | |
In sulfur dioxide |
Conditions | Yield |
---|---|
In water decomposition in water;; |
ethyl sulfate
Conditions | Yield |
---|---|
With hydrogenchloride In water | 91% |
7-mercapto-1,4-benzodioxane-5-carboxylic acid
ethyl sulfate
7-ethylthio-1,4-benzodioxane-5-carboxylic acid
Conditions | Yield |
---|---|
With hydrogenchloride In water | 81% |
ethyl sulfate
7,8-dichloro-6-nitro-4-oxo-1,4-dihydroquinoline
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 60℃; | 60% |
Conditions | Yield |
---|---|
at 120 - 165℃; under 4.50045E-06 Torr; | 43% |
bei der Destillation im Vakuum; | |
With sodium sulfate durch Destillation unter vermindertem Druck; | |
With sodium ethyl sulfate durch Destillation unter vermindertem Druck; | |
bei der Destillation im Vakuum; |
ethyl sulfate
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 20℃; for 12h; | 39% |
ethyl sulfate
Conditions | Yield |
---|---|
With sodium perchlorate; triethylamine In ethanol for 6h; Heating; | 27% |
2(RS)-(2-hydroxyethyl)piperidine
ethyl sulfate
2-(1-ethyl-[2]piperidyl)-ethanol
Conditions | Yield |
---|---|
With water; potassium |
Conditions | Yield |
---|---|
anschliessendes Behandeln mit wss.HClO4; |
Conditions | Yield |
---|---|
With iron(II) sulfate at 140℃; |
ethyl sulfate
1,4-diamino-9,10-anthraquinone
1,4-bisethylamino-anthraquinone
Conditions | Yield |
---|---|
at 140℃; |
Conditions | Yield |
---|---|
With phosphorus pentachloride |
Conditions | Yield |
---|---|
With steam; ammonia | |
With ammonia; water |
Conditions | Yield |
---|---|
With diethyl sulfate; phosphorite; sulfuric acid at 250 - 300℃; | |
With sodium sulfate at 300℃; | |
With sodium chloride at 300℃; |
Conditions | Yield |
---|---|
With hydrogenchloride at 140℃; unter Druck; | |
With hydrogenchloride at 140℃; unter Druck; |
Conditions | Yield |
---|---|
With chromium(VI) oxide; water; iron(III) chloride Electrolysis; | |
With manganese(IV) oxide; water; iron(III) chloride Electrolysis; | |
With chromium(VI) oxide; water; iron(III) chloride Electrolysis; | |
With manganese(IV) oxide; water; iron(III) chloride Electrolysis; |
ethyl sulfate
chloroformic acid ethyl ester
A
diethyl sulfate
B
chloroethane
Conditions | Yield |
---|---|
at 40 - 50℃; | |
at 40 - 50℃; |
Conditions | Yield |
---|---|
With water at 110℃; |
Conditions | Yield |
---|---|
at 50 - 80℃; | |
at 50 - 80℃; |
Conditions | Yield |
---|---|
Einw. von NaNO2-Loesung auf das Reaktionsprodukt; |
Conditions | Yield |
---|---|
In diethyl ether |
1-tert-butylperoxy-ethanol
ethyl sulfate
tert-butyl 1-ethoxy-ethyl peroxide
Conditions | Yield |
---|---|
In diethyl ether |
The Ethyl hydrogen sulfate, with the CAS registry number of 540-82-9, is also known as Sulfethylic acid. It belongs to the product category of Pharmaceutical Intermediates. Its EINECS registry number is 208-758-6. This chemical's molecular formula is C2H6O4S and molecular weight is 126.13164. What's more, its IUPAC name is Ethyl hydrogen sulfate. Additionally, it's incompatible with strong oxidizing agents or metals.
Physical properties about Ethyl hydrogen sulfate are: (1)ACD/LogP: 0.08; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -3.42; (4)ACD/LogD (pH 7.4): -3.42; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 4; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 60.98 Å2; (13)Index of Refraction: 1.453; (14)Molar Refractivity: 23.39 cm3; (15)Molar Volume: 86.4 cm3; (16)Polarizability: 9.27×10-24 cm3; (17)Surface Tension: 51.2 dyne/cm; (18)Density: 1.458 g/cm3.
Preparation of Ethyl hydrogen sulfate: it can be obtained by N-Sulfonoxy-p-chloroacetanilide pyridinium salt. The reaction needs solvent Ethanol at temperature of 40 ℃. The yield is 83%.
When you are using this chemical, please be cautious about it as the following: this chemical is soluble in water and weigh more than water. Besides, heat may be generated by dissolution into water. If this chemical is reacted with water or moist air, toxic, corrosive or flammable gases will be released. What's more, contact with molten substance may cause severe burns to skin and eyes.
You can still convert the following data into molecular structure:
(1) SMILES: O=S(=O)(O)OCC
(2) InChI: InChI=1/C2H6O4S/c1-2-6-7(3,4)5/h2H2,1H3,(H,3,4,5)
(3) InChIKey: KIWBPDUYBMNFTB-UHFFFAOYAR
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