CAS 945-51-7
:Diphenyl sulfoxide
Description:
Diphenyl sulfoxide is an organic compound characterized by the presence of a sulfoxide functional group attached to two phenyl rings. It is typically a colorless to pale yellow liquid with a distinctive odor. The compound is known for its moderate polarity, which allows it to act as a solvent for various organic reactions and processes. Diphenyl sulfoxide exhibits good thermal stability and is soluble in organic solvents such as acetone and ethanol, but has limited solubility in water. Its chemical structure contributes to its utility in various applications, including as a reagent in organic synthesis and as a solvent in electrochemical studies. Additionally, diphenyl sulfoxide can participate in oxidation-reduction reactions, making it valuable in the field of organic chemistry. Safety considerations include handling it with care, as it may cause irritation upon contact with skin or eyes. Overall, diphenyl sulfoxide is a versatile compound with significant relevance in both industrial and laboratory settings.
Formula:C12H10OS
InChI:InChI=1S/C12H10OS/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
InChI key:InChIKey=JJHHIJFTHRNPIK-UHFFFAOYSA-N
SMILES:S(=O)(C1=CC=CC=C1)C2=CC=CC=C2
Synonyms:- (Benzenesulfinyl)benzene
- 1,1'-Sulfinylbis[benzene]
- 1,1'-Sulfinyldibenzene
- Benzene, 1,1'-sulfinylbis-
- Difenil Sulfoxido
- Diphenyl sulfoxide
- Diphenyl sulphoxide
- Diphenylsulfoxid
- Diphenylsulfoxyde
- Nsc 630195
- Nsc 6779
- Phenyl sulphoxide
- Sulfinyldibenzene
- Phenyl sulfoxide
- Diphenyl sulfoxide, 98+%
- DIPHENYL SULFOXIDE PESTANAL
- sulfoxide,diphenyl
- Diphenyl sulfoxide, 97+%
- Sulfoxide, diphenyl
- Diphenyl Sulphoxide 98%
- PhS(O)Ph
- DiphenylSulphoxide98%
- 1,1’-sulfinylbis-benzen
- Phenylsulfinylbenzene
- Diphenylsulphoxide,97%
- Phenyl sulfoxide, 97% 25g
- See more synonyms
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Found 7 products.
Diphenyl sulfoxide, 98+%
CAS:<p>Diphenyl sulfoxide is a reagent used as an oxidant and hydroxyl activator in combination with a variety of electrophilic reagents. Efficient glycosidation of a phenyl thiosialoside donor with diphenyl sulfoxide and triflic anhydride in dichloromethane was reported. Direct glycosylations with 1-hydro</p>Formula:C12H10OSPurity:98+%Color and Shape:White to pale cream, Crystals or powder or crystalline powderMolecular weight:202.27Diphenyl sulphoxide
CAS:<p>Diphenyl sulphoxide</p>Formula:C12H10OSPurity:98%Color and Shape: white to off-white solidMolecular weight:202.27g/molDiphenyl Sulfoxide
CAS:Formula:C12H10OSPurity:>99.0%(GC)Color and Shape:White to Almost white powder to crystalineMolecular weight:202.27Diphenyl sulfoxide
CAS:<p>Diphenyl sulfoxide is a glycosidic bond that is used to synthesize sulfoxides. This molecule has been shown to have the ability to form an intramolecular hydrogen bond, which may be due to its diphenyl group. Diphenyl sulfoxide reacts with rat liver microsomes by the michaelis-menten kinetics. The reaction solution is typically monitored for fluorescence probe, which will indicate the presence of nitrite ions or nitrosyl radicals. Nitrogen atoms can be found in this molecule, which may contribute to its asymmetric synthesis. Metal chelate reactions are also observed in this molecule as a result of the reaction mechanism, producing 2-nitrophenol and 4-nitrophenol.</p>Formula:C12H10OSPurity:Min. 95.5%Color and Shape:White PowderMolecular weight:202.27 g/mol






