Hangzhou Yunuo Chemical Co., Ltd is located in Hangzhou city China. As a global supplier in the chemical industry, Yunuochem is to create added value for customers around the world. Sticking to such business idea of "Good faith wins the busine
Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
Cas:5535-48-8
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Type:Lab/Research institutions
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inquiryhigh purity Storage:Sealed, dry, microtherm , avoid light and smell. Package:meet customer's demand Application:organic synthesis Transportation:by sea or by air Port:shanghai
Phenyl vinyl sulfone CAS 5535-48-8 (Vinylsulfonyl)benzene CAS no 5535-48-8 Phenylvinylsulfone Phenyl vinyl sulfone Manufacturer High quality Best price In stock factory CAS 5535-48-8 Phenyl vinyl sulfone COA TDS price MSDS highly quality an
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inquiryTIANFUCHEM-- 5535-48-8--Phenyl vinyl sulfone in stock Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business relat
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryProduct name:Phenyl vinyl sulfone CAS No:5535-48-8 Appearance: White powder Content:98% Appearance:White powder Storage:Store in cool and dry place, away from sun light. Package:25kg/drum Appl
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inquiryWith our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryBeluga chemical professional supply Phenyl-vinylsulfon CAS 5535-48-8 1. Beluga Chemical has a professional RESEARCH and development team and strong technical force to ensure technical support and research capabilities. 2. Made in China and expor
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The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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Min.Order:1 Gram
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inquiry5535-48-8 Phenyl vinyl sulfoneAppearance:white powder Storage:RT Package:according to customers' requirements Application:pharma Transportation:By air(EMS or EUB or FedEx or TNT ect...) or by sea(FOB or CIF or CNF ect...)or according to your demand.
GMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Phenyl vinyl sulfone Chemical Properties Melting point 67-69 °C (lit.) Boiling point 267.16°C (rough estimate) density 1.2660 (rough estimate) refractive index 1.5090 (estimate) storage temp. Refrigerator (+4°C) solubi
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Type:Lab/Research institutions
inquiryfactory?direct?saleAppearance:White Powder Storage:Store In Dry, Cool And Ventilated Place Package:25kg/drum, also according to the clients requirement Application:It is widely used as a thickener, emulsifier and stabilizer Transportation:By Sea Or B
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inquiryShandong Mopai Biotechnology Co., LTD is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemicals. W
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1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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inquiryConditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20 - 24℃; for 20h; | 100% |
With benzylamine In acetonitrile at 25℃; for 0.525h; Rate constant; different amines, amine concentrations and reaction times; | |
With sodium hydroxide |
Conditions | Yield |
---|---|
With C4H9N2O9W In methanol; water at 20℃; for 4h; chemoselective reaction; | 99% |
With selenium(IV) oxide; dihydrogen peroxide In water; ethyl acetate chemoselective reaction; | 99% |
With dihydrogen peroxide In water at 80℃; for 7.33333h; Catalytic behavior; Reagent/catalyst; Green chemistry; | 98% |
Phenyl vinyl sulfoxide
PVS
Conditions | Yield |
---|---|
With dihydrogen peroxide; [(η5-C5Me5)Mo(CO)3Cl] In acetonitrile at -20 - 20℃; for 4h; | 98% |
With dihydrogen peroxide In water; acetic acid at 20℃; for 12h; | 97% |
With n-C4F9; perfluoro-cis-2,3-dialkyloxaziridine; n-C3F7 In chloroform; trichlorofluoromethane at -20℃; for 0.25h; | 90% |
With dihydrogen peroxide In acetic acid Ambient temperature; Yield given; |
2-(phenylsulfonyl)ethanol
PVS
Conditions | Yield |
---|---|
With methanesulfonyl chloride; triethylamine In dichloromethane at 20℃; for 6h; Dehydration; | 95% |
Multi-step reaction with 2 steps 1: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; DMAP / CH2Cl2 / 12 h / 20 °C 2: aq. NaHCO3 / acetone / 12 h / 20 °C View Scheme | |
Multi-step reaction with 2 steps 1: 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; DMAP / CH2Cl2 / 12 h / 20 °C 2: aq. NaHCO3 / acetone / 12 h / 20 °C View Scheme | |
With sulfuric acid Behandeln des Reaktionsgemisches mit Wasser und mit wss. Natronlauge; |
(1,2-dibromo-ethyl)-phenyl sulfone
PVS
Conditions | Yield |
---|---|
With triphenylphosphine In methanol at 25℃; | 92% |
With triphenylphosphine In methanol at 25℃; Rate constant; | 92% |
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride In dichloromethane for 0.0833333h; Ambient temperature; | 90% |
With PtCl2Styr2; diphenylsilane In chloroform for 4h; Heating; | 15% |
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran | 87% |
With n-butyllithium 1.) hexane, THF, 0 deg C, 0.5 h, 2.) hexane, THF, room temperature; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
In tetrahydrofuran for 0.25h; Cooling with ice; stereospecific reaction; | 85% |
A
PVS
B
phenyl 2-methoxyethyl sulfone
Conditions | Yield |
---|---|
With methanol; triphenylphosphine at 25℃; | A n/a B 82% |
With methanol; triphenylphosphine at 25℃; Rate constant; Thermodynamic data; ΔH(excit.), ΔS(excit.); | A n/a B 82% |
Conditions | Yield |
---|---|
With methanol; triphenylphosphine at 25℃; | A 80% B n/a |
With methanol; triphenylphosphine at 25℃; Rate constant; Thermodynamic data; ΔH(excit.), ΔS(excit.); | A 80% B n/a |
Conditions | Yield |
---|---|
With methanol; triphenylphosphine at 25℃; | A n/a B 78% |
With methanol; triphenylphosphine at 25℃; Rate constant; Thermodynamic data; other β-substituted α-bromosulfones; ΔH(excit.), ΔS(excit.); | A n/a B 78% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 80℃; for 24h; | 78% |
In N,N-dimethyl-formamide at 80℃; Inert atmosphere; | 50% |
In N,N-dimethyl-formamide at 80℃; Inert atmosphere; | 50% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; | 76% |
Conditions | Yield |
---|---|
With palladium dichloride In dimethyl sulfoxide at 50℃; for 8h; chemoselective reaction; | 71% |
Conditions | Yield |
---|---|
Stage #1: sodium benzenesulfonate; 2-bromoethanol In N,N-dimethyl-formamide at 80℃; Inert atmosphere; Stage #2: With methanesulfonyl chloride; triethylamine In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; | 70% |
Conditions | Yield |
---|---|
With oxygen; copper(l) chloride; lithium bromide In dimethyl sulfoxide at 100℃; under 760.051 Torr; for 12h; Schlenk technique; stereoselective reaction; | 67% |
Conditions | Yield |
---|---|
With C36H27CuN8O2; dihydrogen peroxide In methanol; dichloromethane at 0℃; for 10h; | A 52% B 25% |
With dihydrogen peroxide; titanium(IV) isopropylate; L-Tartaric acid; silica gel In methanol; water at 25℃; for 24h; Title compound not separated from byproducts; | A 3% B 94 % Spectr. |
With dihydrogen peroxide; Mg-Al-LDH-WO4 at 20℃; for 3h; |
Conditions | Yield |
---|---|
With pyridine; thionyl chloride; sodium hydrogencarbonate In toluene | A n/a B 0.7% |
Conditions | Yield |
---|---|
With benzene |
Conditions | Yield |
---|---|
Yield given. Multistep reaction; |
thiophenolate
sodium ethanolate
A
cyanide(1-)
B
PVS
C
2-ethoxyethyl phenyl sulphone
D
(2-Isocyano-ethylsulfanyl)-benzene
Conditions | Yield |
---|---|
Rate constant; Product distribution; multistep reaction, 1.) ethanol, 25 deg C; 2.) ethanol; |
Conditions | Yield |
---|---|
With sodium hydroxide for 10h; Ambient temperature; other concentration of NaOH, reaction velocity; |
S-<2-(4-Ethoxycarbonylphenylsulfonyl)ethyl>cystein-methylester
A
L-Cysteine methyl ester
B
PVS
Conditions | Yield |
---|---|
With sodium hydroxide Ambient temperature; reaction times, various conc. of NaOH; |
N-Acetyl-S-<2-(4-ethoxycarbonylphenylsulfonyl)ethyl>cystein
A
N-acetylcystein
B
PVS
Conditions | Yield |
---|---|
With sodium hydroxide Ambient temperature; reaction times, various conc. of NaOH, add. of N-Acetyl-S-<2-(phenylsulfonyl)ethyl>-cystein; |
Conditions | Yield |
---|---|
With sodium hydroxide for 0.5h; Ambient temperature; other concentration of NaOH, reaction velocity; |
N-(Benzyloxycarbonyl)glycyl-S-<2-(phenylsulfonyl)ethyl>cystein-methylester
A
PVS
B
N-(Benzyloxycarbonyl)glycyl-cystein-methylester
Conditions | Yield |
---|---|
With sodium hydroxide for 1.75h; Ambient temperature; reaction velocity; |
Conditions | Yield |
---|---|
With triethylamine 1.) ethanol, reflux, 3 d; 2.) dichloromethane, ethanol, reflux; Yield given. Multistep reaction; |
A
PVS
Conditions | Yield |
---|---|
With sodium hydroxide In methanol for 1.75h; Product distribution; Ambient temperature; |
A
PVS
B
cysteine methyl ester hydrochloride
Conditions | Yield |
---|---|
With sodium hydroxide; triethylamine In methanol for 10h; Product distribution; Ambient temperature; |
Conditions | Yield |
---|---|
In acetonitrile for 2h; Ambient temperature; | 100% |
Stage #1: 1H-imidazole With o-phenylenebis(diphenylphosphine); potassium tert-butylate; copper(l) chloride In toluene for 0.166667h; Michael Addition; Inert atmosphere; Stage #2: PVS In toluene at 22℃; for 3h; Michael Addition; Inert atmosphere; | 99% |
N-methylmaleimide
Cyclohexanone oxime
PVS
2,2-spiropentamethylene-3-(2'-phenylsulphonylethyl)-7-methyl-3,7-diaza-4-oxabicyclo<3.3.0>octane-6,8-dione
Conditions | Yield |
---|---|
In [D3]acetonitrile for 720h; Ambient temperature; | 100% |
PVS
1-(adamantane-1-carbonyloxy)pyridine-2(1H)-thione
2-(1-adamantyl)-1-phenylsulphonyl-1-(pyridine-2-thiyl)ethane
Conditions | Yield |
---|---|
In dichloromethane; benzene for 0.166667h; Mechanism; Ambient temperature; Irradiation; easy formation of a carbon-carbon bond by simply incorporating activated olefin into the system (further activated olefins gave similar products); | 100% |
In dichloromethane; benzene for 0.166667h; Ambient temperature; Irradiation; during work up excess monomer was destroyed by hydrazine; | 100% |
PVS
diacetone acrylamide oxime
2-(2-phenylsulphonylethyl)-1,8,8-trimethyl-6-oxo-2,7-diaza-3-oxabicyclo<4.3.0>nonane
Conditions | Yield |
---|---|
In xylene for 16h; Heating; | 100% |
In xylene at 140℃; Yield given; |
PVS
2-(1-adamantyl)-1-phenylsulphonyl-1-(pyridine-2-thiyl)ethane
Conditions | Yield |
---|---|
In dichloromethane; benzene at 20 - 25℃; for 0.166667h; Irradiation; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
In ethanol at 20℃; Cooling with ice; | 81% |
Conditions | Yield |
---|---|
With water; sodium chloride In acetonitrile pH=2; Electrochemical reaction; Green chemistry; | 100% |
With N-ethylpiperidine hypophosphite; triethyl borane; oxygen In 1,4-dioxane at 20℃; for 1h; | 98% |
With cetyltrimethylammonim bromide; 4,4'-dicyano-4,4'-azo-di-valeric acid; N-ethylpiperidinium hypophosphite In 1,4-dioxane; water at 100℃; for 0.5h; | 94% |
With (CH3)3N(+)(CH2)15CH3*H2PO2(-); 4,4'-dicyano-4,4'-azo-di-valeric acid In water at 100℃; for 1h; | 89% |
With tert-butylisonitrile; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; triethylamine; lithium chloride; palladium dichloride In benzene for 16h; Giese Free Radical Synthesis; Irradiation; Inert atmosphere; | 88% |
Conditions | Yield |
---|---|
With hydrogenchloride; water; sodium chloride In acetonitrile for 20h; pH=2; Solvent; pH-value; Electrochemical reaction; Green chemistry; | 100% |
With 2,2'-azobis(isobutyronitrile); tert-butyl(2,6-dimethoxy-1-methylcyclohexa-2,5-dien-1-yl)dimethylsilane In hexane for 14h; Giese-type addition; Heating; | 89% |
With indium In methanol; water at 20℃; for 0.5h; | 86% |
Conditions | Yield |
---|---|
With quinidine 9-O-(9'-phenanthryl)ether In toluene at 20℃; for 36h; Michael addition; optical yield given as %ee; enantioselective reaction; | 100% |
PVS
3-methoxybenzenethiol
2-[(3-methoxyphenyl)sulfanyl]ethyl phenyl sulfone
Conditions | Yield |
---|---|
With potassium carbonate In dichloromethane at 20℃; for 20h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
PVS
N,N',N'-trimethylenediamine
N1,N1,N2-trimethyl-N2-[2-(phenylsulfonyl)ethyl]-1,2-ethanediamine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
(R)-sec-butylamine
PVS
(R)-N-[2-(phenylsulfonyl)ethyl]butan-2-amine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
In ethanol at 0 - 20℃; | 99% |
PVS
propan-1-ol-3-amine
3-[(2-(phenylsulfonyl)ethyl)amino]propan-1-ol
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
1-methyl-piperazine
PVS
1-methyl-4-[2-(phenylsulfonyl)ethyl]piperazine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
PVS
N,N-dimethylethylenediamine
N1,N1-dimethyl-N2-[2-(phenylsulfonyl)ethyl]ethane-1,2-diamine
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 100% |
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydroxide In ethanol; water at 20℃; for 2h; Michael Addition; Green chemistry; | 99% |
triethylamine In tetrahydrofuran for 4.5h; Ambient temperature; | 96% |
With potassium carbonate In dichloromethane at 20℃; for 20h; Inert atmosphere; | 92% |
With 1,3-dicyclohexylimidazolium-2-carboxylate In tetrahydrofuran at 21℃; for 2h; Michael Addition; | 90% |
Conditions | Yield |
---|---|
Stage #1: aniline With potassium tert-butylate; bis[2-(diphenylphosphino)phenyl] ether; copper(l) chloride In toluene for 0.166667h; Michael Addition; Inert atmosphere; Stage #2: PVS In toluene at 22℃; for 3h; Reagent/catalyst; Michael Addition; Inert atmosphere; | 99% |
acetic acid at 200℃; for 0.333333h; Michael addition; microwave irradiation; | 96% |
With acetic acid at 200℃; for 0.333333h; Microwave irradiation; Sealed vessel tube; | 76% |
N-tert-Butylhydroxylamine
PVS
Conditions | Yield |
---|---|
In dichloromethane for 2h; Ambient temperature; | 99% |
PVS
1-methoxy-3-<(phenylthio)methyl>-1,3-butadiene
C20H22O3S2
Conditions | Yield |
---|---|
With hydroquinone In toluene at 110℃; for 48h; | 99% |
Conditions | Yield |
---|---|
With cyclohexa-1,4-diene In dichloromethane at 30℃; for 0.25h; Irradiation; | 99% |
With cyclohexa-1,4-diene In dichloromethane at 30℃; for 3h; Irradiation; | 93% |
PVS
3-Adamantan-1-yl-4-tert-butyl-thiophene 1,1-dioxide
Conditions | Yield |
---|---|
In 1,2-dichloro-benzene for 27.5h; Heating; | 99% |
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