p-β-bromoethylbenzenesulfonic acid
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
With sodium hydroxide; sodium nitrite In water at 90℃; for 4h; Autoclave; Large scale; |
p-β-bromoethylbenzenesulfonic acid
B
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
With sodium hydroxide; sodium nitrite In water at 105℃; for 1h; Inert atmosphere; Autoclave; |
Conditions | Yield |
---|---|
With thionyl chloride; 2,6-di-tert-butyl-4-methyl-phenol In N,N-dimethyl-formamide for 27h; Cooling; | 100% |
With thionyl chloride In N,N-dimethyl-formamide for 27h; | 95% |
With thionyl chloride In N,N-dimethyl-formamide; acetonitrile at 70℃; for 3h; Inert atmosphere; Cooling with ice; | 82% |
sodium 4-styrenesulfonate
benzyltri(n-butyl)ammonium chloride
4-vinylbenzenesulfonic acid benzyltributylammonium salt
Conditions | Yield |
---|---|
In water at 20℃; for 0.0833333h; | 100% |
In dichloromethane; water at 20℃; for 0.5h; | 99% |
In dichloromethane; water | 85% |
sodium 4-styrenesulfonate
C11H19N2(1+)*C8H7O3S(1-)
Conditions | Yield |
---|---|
In water at 20℃; | 98% |
Conditions | Yield |
---|---|
In dichloromethane; water | 98% |
sodium 4-styrenesulfonate
N,N-dimethyl-n-octadecylammonium p-styrenesulfonate
Conditions | Yield |
---|---|
In chloroform; water for 0.5h; | 97.5% |
sodium 4-styrenesulfonate
(8S,9R)-(-)-N-benzylcinchonidinium chloride
N-9-benzylcinchonidinium p-styrenesulfonate
Conditions | Yield |
---|---|
In dichloromethane; water | 97% |
sodium 4-styrenesulfonate
tetra-n-butylphosphonium chloride
tetrabutylphosphonium p-styrenesulfonate
Conditions | Yield |
---|---|
In water at 20℃; for 48h; | 97% |
In water at 20℃; for 24h; |
sodium 4-styrenesulfonate
dimethyldioctadecylammonium bromide
dioctadecyldimethylammonium p-styrenesulfonate
Conditions | Yield |
---|---|
In water at 70℃; | 95% |
sodium 4-styrenesulfonate
C21H39N2(1+)*C8H7O3S(1-)
Conditions | Yield |
---|---|
In methanol; water at 20℃; | 95% |
Conditions | Yield |
---|---|
In dichloromethane; water | 95% |
tetrabutylammomium bromide
sodium 4-styrenesulfonate
tetrabutylammonium 4-vinylbenzenesulfonate
Conditions | Yield |
---|---|
In water; acetone at 20℃; for 6h; Inert atmosphere; | 95% |
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
In water at 20℃; for 24h; | 94% |
sodium 4-styrenesulfonate
1-vinyl-3-octadecylimidazolium p-styrenesulphonate
Conditions | Yield |
---|---|
In water at 20℃; for 48h; | 91.9% |
In water at 20℃; for 48h; |
tetrabutyl-ammonium chloride
sodium 4-styrenesulfonate
tetrabutylammonium 4-vinylbenzenesulfonate
Conditions | Yield |
---|---|
In dichloromethane; water | 90% |
Conditions | Yield |
---|---|
With N-Bromosuccinimide; water; 1,8-diazabicyclo[5.4.0]undec-7-ene at 60℃; under 12929 Torr; for 6h; Product distribution / selectivity; | 89% |
With water; dihydrogen peroxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; tetrabutylammomium bromide at 45 - 55℃; under 12929 Torr; for 15h; Product distribution / selectivity; | 89% |
sodium 4-styrenesulfonate
N-9-anthracenylmethylcinchonidinium p-styrenesulfonate
Conditions | Yield |
---|---|
In dichloromethane; water | 89% |
Conditions | Yield |
---|---|
In water at 20℃; | 83% |
In water at 20℃; |
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
With D-glucose; oxygen; glucose oxidase; further reagents In phosphate buffer; water-d2 for 3h; pH=7.0; Product distribution; Further Variations:; Reagents; concentrations; | 81% |
With magnesium monoperoxyphthalate hexahydrate In water-d2 for 1.5h; Product distribution; Ambient temperature; add of meso-tetrakis-(4-N-methylpyridyl)porphyrinatomanganese(III) chloride, Mn(III)TPPS or CoTMPyP: efficient cat. effect; pH 6.5-6.8 (phosphate buffer); var. time.; | |
With Oxone; chloro(meso-tetra(4-N-methylpyridinio)porphyrinato)manganese(III)(4+) In water-d2 for 0.0333333h; Ambient temperature; pH 6.8 (phosphate buffer); Yield given; | |
With magnesium monoperoxyphthalate hexahydrate In water-d2 for 15h; Ambient temperature; pH 6.5 (phosphate buffer); Yield given; | |
With C30H24F3FeN5O(2+) In water at 25℃; pH=5.5; Kinetics; Reagent/catalyst; |
Conditions | Yield |
---|---|
In dichloromethane; water | 81% |
sodium 4-styrenesulfonate
1-(4-vinylbenzyl)thymine
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In water; isopropyl alcohol at 65℃; for 15h; | 80% |
Conditions | Yield |
---|---|
With palladium diacetate; triethylamine; tris-(o-tolyl)phosphine In water; N,N-dimethyl-formamide at 100℃; for 2h; Heck Reaction; | 80% |
Conditions | Yield |
---|---|
at 95℃; for 1.5h; | 78% |
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
In methanol at 20℃; | 75% |
Conditions | Yield |
---|---|
Stage #1: sodium 4-styrenesulfonate With silver nitrate In water at 0℃; for 2h; Stage #2: ethyl bromide In acetonitrile at 70℃; for 15h; | 70% |
With silver nitrate In water; acetonitrile at 0 - 70℃; | 67% |
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
In acetonitrile at 45℃; for 72h; | 67% |
Conditions | Yield |
---|---|
With trifluoroacetic acid In water at 30℃; for 72h; Temperature; Schlenk technique; Inert atmosphere; | 66% |
Conditions | Yield |
---|---|
Stage #1: sodium 4-styrenesulfonate With thionyl chloride In N,N-dimethyl-formamide; toluene at 100℃; for 2h; Stage #2: Cyclopropylamine In dichloromethane at 20℃; for 1h; | 46.2% |
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
With sulfuric acid In water for 16h; Reflux; | 34% |
Ni(II)dibromoporphyrin
sodium 4-styrenesulfonate
Conditions | Yield |
---|---|
With PPh3; Pd(OAc)2; K2CO3 In N,N-dimethyl-formamide Ni(II) dibromoporphyrin reacted with sodium 4-styrenesulfonate in DMF/xylene in presence of PPh3, Pd(OAc)2 and K2CO3; NMR, MS; | 26% |
sodium 4-styrenesulfonate
ethyl piperidine-2-carboxylate hydrochloride
Conditions | Yield |
---|---|
Stage #1: sodium 4-styrenesulfonate With oxalyl dichloride In DMF (N,N-dimethyl-formamide) at 20℃; for 2.5h; Stage #2: ethyl piperidine-2-carboxylate hydrochloride With triethylamine In dichloromethane at 20℃; for 16h; | 19% |
The Sodium p-styrenesulfonate, with the CAS registry number 2695-37-6, is also known as Styrene-4-sulfonic acid sodium salt. It belongs to the product category of Aromatic Esters. Its EINECS number is 220-266-3. This chemical's molecular formula is C8H7NaO3S and molecular weight is 206.19. What's more, its systematic name is Sodium 4-vinylbenzenesulfonate. This chemical should be sealed and stored in a cool and dry place. It is used as dyeing modifier, reactive emulsifier and electroplating luster agent.
Physical properties of Sodium p-styrenesulfonate are: (1)ACD/LogP: 0.951; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -2.55; (4)ACD/LogD (pH 7.4): -2.55; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4): 1.00; (9)#H bond acceptors: 3; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 62.75 Å2.
Uses of Sodium p-styrenesulfonate: it can be used to produce p-styrenesulfonyl chloride. It will need reagent SOCl2 and solvent dimethylformamide with the reaction time of 27 hours. The yield is about 95%.
When you are using this chemical, please be cautious about it as the following:
This chemicalis irritating to eyes, respiratory system and skin. It is harmful if swallowed. It has a risk of serious damage to eyes. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical When using it, you need wear suitable protective clothing, gloves and eye/face protection.
You can still convert the following datas into molecular structure:
(1)SMILES: [Na+].O=S([O-])(=O)c1ccc(\C=C)cc1
(2)Std. InChI: InChI=1S/C8H8O3S.Na/c1-2-7-3-5-8(6-4-7)12(9,10)11;/h2-6H,1H2,(H,9,10,11);/q;+1/p-1
(3)Std. InChIKey: XFTALRAZSCGSKN-UHFFFAOYSA-M
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