Conditions | Yield |
---|---|
hydrolysis at pH 11; |
2-hydroxyethane-1-sulfonyl chloride
A
sodium 2-hydroxyethanesulfonate
B
sodium vinylsulfonate
C
Na-salt of 2-chloroethane-1-sulfonic acid
Conditions | Yield |
---|---|
With sodium hydroxide; potassium chloride at 25℃; pH 4; | A 52 % Spectr. B n/a C 48 % Spectr. |
Conditions | Yield |
---|---|
With hydroxide In water at 10℃; under 1.66513E-07 Torr; Rate constant; var. pressure values, var. solvents and temperatures; |
Conditions | Yield |
---|---|
With N2 catalyst, 80°C, under pressure; | |
With nitrogen catalyst, 80°C, under pressure; |
Conditions | Yield |
---|---|
With sodium sulfate; calcium hydroxide In water at 35 - 80℃; for 1h; pH=10 - 11; | |
With sodium sulfate; calcium hydroxide In water at 35 - 80℃; for 1h; pH=7-11; |
Conditions | Yield |
---|---|
With sulfur trioxide; sodium hydroxide at 20 - 60℃; for 8h; Large scale; |
Conditions | Yield |
---|---|
With water at 120℃; for 12h; Michael-type addition reaction; | 98% |
Conditions | Yield |
---|---|
With strongly-acidic ion-exchange resin DOWEXMonosphere 650C In water Product distribution / selectivity; | 97% |
With sodium hydroxide In water for 4h; | 86.7% |
With water Product distribution / selectivity; |
sodium vinylsulfonate
ethylenediamine
sodium 2-[(2-aminoethyl)amino]ethanesulphonate
Conditions | Yield |
---|---|
at 30℃; for 5h; Reflux; | 92.11% |
In water for 24h; Reflux; | 0.91 g |
Conditions | Yield |
---|---|
In methanol at 120℃; for 48h; Autoclave; | 90% |
Conditions | Yield |
---|---|
With sodium hydroxide for 24h; Heating; | 89% |
Conditions | Yield |
---|---|
In methanol; water at 120℃; for 48h; Inert atmosphere; | 86% |
sodium vinylsulfonate
N1-(3-Amino-propyl)-N1-(3-{{3-[bis-(3-amino-propyl)-amino]-propyl}-[2-(bis-{3-[bis-(3-amino-propyl)-amino]-propyl}-amino)-ethyl]-amino}-propyl)-propane-1,3-diamine
Conditions | Yield |
---|---|
In methanol at 120℃; for 48h; Autoclave; | 85% |
sodium vinylsulfonate
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In water for 72h; Michael Addition; Reflux; | 85% |
Conditions | Yield |
---|---|
In water at 60℃; for 6h; Large scale; | 85% |
sodium vinylsulfonate
Conditions | Yield |
---|---|
With sodium hydroxide Heating; | 84% |
Conditions | Yield |
---|---|
With acetic acid In methanol; water at 25 - 100℃; for 3 - 170h; Product distribution / selectivity; | 82% |
sodium vinylsulfonate
N-phenylphenylene-1,4-diamine
A
N-(4-anilino)phenyl-vinylsulfonamide
B
vinylsulfonyl chloride
Conditions | Yield |
---|---|
With phosphorus pentachloride; triethylamine In toluene | A 81% B n/a |
sodium vinylsulfonate
2,2'-iminobis[ethanol]
sodium N,N-bis(2-hydroxyethyl)-2-aminoethanesulfonate
Conditions | Yield |
---|---|
for 24h; Reflux; | 81% |
Conditions | Yield |
---|---|
In ethanol; water at 120℃; for 72h; Michael Addition; | 80% |
Conditions | Yield |
---|---|
With 2,2-dimethoxy-2-phenylacetophenone In tetrahydrofuran; methanol for 4h; UV-irradiation; | 80% |
sodium vinylsulfonate
Conditions | Yield |
---|---|
In methanol; water at 120℃; for 48h; Inert atmosphere; | 78% |
Conditions | Yield |
---|---|
In methanol at 120℃; for 48h; Autoclave; | 78% |
sodium vinylsulfonate
Conditions | Yield |
---|---|
With sodium hydroxide Heating; | 74% |
Conditions | Yield |
---|---|
In water for 20h; Reflux; | 74% |
sodium vinylsulfonate
Conditions | Yield |
---|---|
In methanol; water at 120℃; for 48h; Inert atmosphere; | 73% |
In ethanol; water at 120℃; for 72h; Michael Addition; | 73% |
Conditions | Yield |
---|---|
With sodium acetate; trans-di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide at 100℃; for 18h; Heck reaction; | 70% |
Conditions | Yield |
---|---|
With 2,2-dimethoxy-2-phenylacetophenone In tetrahydrofuran; methanol; water for 3h; UV-irradiation; | 70% |
Conditions | Yield |
---|---|
In methanol; water at 120℃; for 48h; Inert atmosphere; | 65% |
Conditions | Yield |
---|---|
In methanol; water at 120℃; for 48h; Inert atmosphere; | 63% |
In water Michael Addition; | 57% |
2-hydroxy-3-iodonaphthalene-1,4-dione
sodium vinylsulfonate
Conditions | Yield |
---|---|
With palladium diacetate; potassium carbonate In water for 2h; Heck reaction; Heating; | 62% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; horseradish peroxidase In water at 20℃; for 24h; | 36% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; horseradish peroxidase In water at 20℃; for 48h; | 36% |
Conditions | Yield |
---|---|
With dihydrogen peroxide; horseradish peroxidase In water at 25℃; for 24h; | 36% |
(R)-1-phenyl-ethyl-amine
sodium vinylsulfonate
sodium (R)-2-(1-phenylethylamino)ethanesulfonate
Conditions | Yield |
---|---|
In water for 120h; Reflux; | 25% |
The ethenesulfonic acid,sodium salt (1:1), with the CAS register number 3039-83-6, has other names as ethenesulfonicacid,sodiumsalt; ethylenesulfonic acid sodium salt; sodium vinylsulfonate; sodium vinylsulphonate; sodium ethylenesulfonate; sodium ethylenesulphonate; vinyl sulfonate, sodium salt; vinylsulfonic acid sodium salt.
The physical characteristics could be summarized as: (1)ACD/LogP: -0.30; (2)ACD/LogD(pH5.5): -3.8; (3)ACD/LogD(pH7.4): -3.8; (4)ACD/BCF(pH5.5): 1; (5)ACD/BCF(pH7.4): 1; (6)ACD/KOC(pH5.5): 1; (7)ACD/KOC(pH7.4): 1; (8)#Hbondacceptors: 3; (9)#Hbonddonors: 1; (10)#FreelyRotatingBonds: 1; (11)PolarSurfaceArea: 62.75.
This chemical is often supplied as a concentrated (30%) aqueous solution, deep yellow-brown in colour, and it is sensitive to light and is stable in air while incompatible with strong oxidizing agents.
Being a kind of irritant chemical, it is harmful to eyes, respiratory system and skin and may cause sensitisation by inhalation and skin contact. So while dealing with this chemical, you should follow the below instructions. Wear suitable protective clothing, gloves and eye/face protection. If in case of contact with eyes, rinse immediately with plenty of water and seek medical advice. And after contacting with skin, wash immediately with plenty of ... (to be specified by the manufacturer).
As for its usage, it is often applied in the synthesis of some propionyl and also be usde in synthetic fibre and monomer conversion of various polymer. Besides, it could be used as the electroplate brightener, surface active agent and pharmaceutic intermediates.
In addition, you could refer to the following data information to get the molecular structure:
SMILES:[Na+].[O-]S(=O)(=O)\C=C
InChI:InChI=1/C2H4O3S.Na/c1-2-6(3,4)5;/h2H,1H2,(H,3,4,5);/q;+1/p-1
InChIKey:BWYYYTVSBPRQCN-REWHXWOFAC
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