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Details
Cosmetics Grade Allyl phenyl sulfone 16212-05-8 For Sale with Good Price
- Molecular Formula: C9H10O2S
- Molecular Weight: 182.243
- Appearance/Colour: Clear colourless to faintly yellow liquid
- Vapor Pressure: 0.000456mmHg at 25°C
- Refractive Index: n20/D 1.548(lit.)
- Boiling Point: 324.7 °C at 760 mmHg
- Flash Point: 182.2 °C
- PSA： 42.52000
- Density: 1.143 g/cm3
- LogP: 2.72710
Allyl phenyl sulfone(Cas 16212-05-8) Usage
InChI:InChI=1/C9H10O2S/c1-2-8-12(10,11)9-6-4-3-5-7-9/h2-7H,1,8H2
16212-05-8 Relevant articles
A convenient method for the synthesis of β,γ-unsaturated sulfones through zinc-mediated C-S coupling reaction
Sun, Peipei,Wang, Lei,Zhang, Yongmin
, p. 5549 - 5550 (1997)
Through zinc-mediated coupling reaction ...
A new attachment/cleavage strategy: Polymer-bound allylic sulfones in a solid-phase route to trisubstituted olefins
Halm, Chris,Evarts, Jerry,Kurth, Mark J.
, p. 7709 - 7712 (1997)
By tethering allyl sulfone to polystyren...
Organic oxidations promoted in vortex driven thin films under continuous flow
Pye, Scott J.,Dalgarno, Scott J.,Chalker, Justin M.,Raston, Colin L.
, p. 118 - 124 (2018)
With increasing concerns for the environ...
Design, Multigram Synthesis, and in Vitro and in Vivo Evaluation of Propylamycin: A Semisynthetic 4,5-Deoxystreptamine Class Aminoglycoside for the Treatment of Drug-Resistant Enterobacteriaceae and Other Gram-Negative Pathogens
Matsushita, Takahiko,Sati, Girish C.,Kondasinghe, Nuwan,Pirrone, Michael G.,Kato, Takayuki,Waduge, Prabuddha,Kumar, Harshitha Santhosh,Sanchon, Adrian Cortes,Dobosz-Bartoszek, Malgorzata,Shcherbakov, Dimitri,Juhas, Mario,Hobbie, Sven N.,Schrepfer, Thomas,Chow, Christine S.,Polikanov, Yury S.,Schacht, Jochen,Vasella, Andrea,B?ttger, Erik C.,Crich, David
, p. 5051 - 5061 (2019)
Infectious diseases due to multidrug-res...
Highly porous conjugated polymers for selective oxidation of organic sulfides under visible light
Wang, Zi Jun,Ghasimi, Saman,Landfester, Katharina,Zhang, Kai A. I.
, p. 8177 - 8180 (2014)
High surface area porous conjugated poly...
Polyvinylpolypyrrolidone-supported boron trifluoride (PVPP-BF3): Highly efficient catalyst for chemoselective oxygenation of sulfides to sulfones by H2O2
Mokhtary, Masoud,Lakouraj, Moslem Mansour,Niaki, Masoumeh Rastegar
, p. 321 - 326 (2012)
A highly efficient method for the oxidat...
Oxidation of sulfides including DBT using a new vanadyl complex of a non-innocent o-aminophenol benzoxazole based ligand
Saeedi, Roonak,Safaei, Elham,Lee, Yong-Ill,Lu?nik, Janez
, (2019)
Reaction of a non-innocent o-aminophenol...
Indium-mediated Coupling Reaction of Sulfonyl Chlorides with Alkyl Bromides in Water. A Facile Synthesis of Sulfones
Wang, Lei,Zhang, Yongmin
, p. 588 - 589 (1998)
Indium-mediated coupling of alkyl bromid...
A convenient synthesis of sulfones using zinc mediated coupling reaction of sulfonyl chlorides with alkyl halides in aqueous media
Sun, Xinghua,Wang, Lei,Zhang, Yongmin
, p. 1785 - 1791 (1998)
An efficient procedure for the preparati...
COMPOSITES, METHODS AND USES THEREOF
-
Page/Page column 22-23, (2021/06/04)
The present invention relates, in genera...
Polyoxometalate-Based Organic-Inorganic Hybrids as Heterogeneous Catalysts for Cycloaddition of CO2with Epoxides and Oxidative Desulfurization Reactions
Zhao, Yu-Qing,Liu, Ying-Ying,Ma, Jian-Fang
, p. 1019 - 1027 (2021/01/13)
Self-assembly of polyoxometalates, trans...
Assembly of polyoxometalate-thiacalix[4]arene-based inorganic-organic hybrids as efficient catalytic oxidation desulfurization catalysts
Li, Jie,Du, Peng,Liu, Ying-Ying,Ma, Jian-Fang
supporting information, p. 1349 - 1356 (2021/02/09)
Self-assembly of polyoxometalates, Ni(ii...
Silver-catalyzed decarboxylative radical allylation of α,α-difluoroarylacetic acids for the construction of CF2-allyl bonds
Wang, Pingyang,Du, Pengcheng,Sun, Qianqian,Zhang, Jianhua,Deng, Hongmei,Jiang, Haizhen
supporting information, p. 2023 - 2029 (2021/03/16)
An efficient silver-catalyzed method of ...
16212-05-8 Process route
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-
5296-64-0
allyl phenyl thioether
-
-
98-09-9
benzenesulfonyl chloride
-
-
16212-05-8
(allylsulfonyl)benzene
-
-
138918-58-8
1-Chloro-2,3-bis(phenylthio)propane
-
-
138918-57-7
(2-chloropropane-1,3-diyl)bis(phenylsulfane)
-
-
882-33-7
diphenyldisulfane
| Conditions | Yield |
|---|---|
|
tris(triphenylphosphine)ruthenium(II) chloride;
In
benzene;
at 140 ℃;
for 24h;
|
2 % Chromat.
54 % Chromat. 18 % Chromat. 71 % Chromat. |
-
-
5296-64-0
allyl phenyl thioether
-
-
16212-05-8
(allylsulfonyl)benzene
-
-
19093-37-9
allyl phenyl sulfoxide
-
-
882-33-7
diphenyldisulfane
| Conditions | Yield |
|---|---|
|
With
Zeolite Y; doped with methylene blue; oxygen;
In
hexane;
for 1h;
Photolysis;
|
16212-05-8 Upstream products
-
5296-64-0
allyl phenyl thioether
-
873-55-2
sodium benzenesulfonate
-
106-95-6
allyl bromide
-
556-56-9
allyl iodid
16212-05-8 Downstream products
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28975-80-6
Phenyl-propenyl-sulfon
-
2674-25-1
[(2,3-dibromopropyl)sulfonyl]benzene
-
28691-72-7
(E)-1-propenyl phenyl sulfone
-
77657-92-2
2-bromo-1-(phenylsulfonyl)propane
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