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Diphenyl sulfoxide, 98+%
CAS: 945-51-7 | C12H10OS | 202.271 g/mol
$100.22 - $1095.27
Chemical Identifiers
| CAS | 945-51-7 |
|---|---|
| Molecular Formula | C12H10OS |
| Molecular Weight (g/mol) | 202.271 |
| MDL Number | MFCD00002085 |
| InChI Key | JJHHIJFTHRNPIK-UHFFFAOYSA-N |
| Synonym | diphenyl sulfoxide, phenyl sulfoxide, sulfinyldibenzene, phenylsulfinylbenzene, diphenyl sulphoxide, sulfoxide, diphenyl, diphenylsulfoxide, benzene, 1,1'-sulfinylbis, 1,1'-sulfinyldibenzene, phenylsulfinyl benzene |
| PubChem CID | 13679 |
| IUPAC Name | benzenesulfinylbenzene |
| SMILES | C1=CC=C(C=C1)S(=O)C2=CC=CC=C2 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAB2213514
|
Thermo Scientific Chemicals
B2213514 |
25 g |
Each for $100.22
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AAB2213522
|
Thermo Scientific Chemicals
B2213522 |
100 g |
Each for $272.03
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AAB2213536
|
Thermo Scientific Chemicals
B2213536 |
500 g |
Each for $1,095.27
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Description
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-hydroxy glycosyl donors is made using trifluoromethanesulfonic anhydride and diphenyl sulfoxide. The preparation of triarylsulfonium halides was by the action of aryl Grignard reagents on diphenyl sulfoxide.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsDiphenyl 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-hydroxy glycosyl donors is made using trifluoromethanesulfonic anhydride and diphenyl sulfoxide. The preparation of triarylsulfonium halides was by the action of aryl Grignard reagents on diphenyl sulfoxide.
Solubility
Soluble in water. Soluble in most organic solvents.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
Chemical Identifiers
| 945-51-7 | |
| 202.271 | |
| JJHHIJFTHRNPIK-UHFFFAOYSA-N | |
| 13679 | |
| C1=CC=C(C=C1)S(=O)C2=CC=CC=C2 |
| C12H10OS | |
| MFCD00002085 | |
| diphenyl sulfoxide, phenyl sulfoxide, sulfinyldibenzene, phenylsulfinylbenzene, diphenyl sulphoxide, sulfoxide, diphenyl, diphenylsulfoxide, benzene, 1,1'-sulfinylbis, 1,1'-sulfinyldibenzene, phenylsulfinyl benzene | |
| benzenesulfinylbenzene |
Specifications
| 945-51-7 | |
| 206°C to 208°C (13 mmHg) | |
| MFCD00002085 | |
| 1908444 | |
| Soluble in water. Soluble in most organic solvents. | |
| C1=CC=C(C=C1)S(=O)C2=CC=CC=C2 | |
| 202.271 | |
| 202.28 | |
| Diphenyl sulfoxide |
| 69°C to 72°C | |
| C12H10OS | |
| 25 g | |
| diphenyl sulfoxide, phenyl sulfoxide, sulfinyldibenzene, phenylsulfinylbenzene, diphenyl sulphoxide, sulfoxide, diphenyl, diphenylsulfoxide, benzene, 1,1'-sulfinylbis, 1,1'-sulfinyldibenzene, phenylsulfinyl benzene | |
| JJHHIJFTHRNPIK-UHFFFAOYSA-N | |
| benzenesulfinylbenzene | |
| 13679 | |
| ≥98% |
Safety and Handling
EINECSNumber : 213-415-9
RTECSNumber : DA9185000
TSCA : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only