| Weight | 324.486 g/mol |
|---|---|
| Formula | C18H28O3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 10 |
Sulfoxide (120-62-7)
sulphoxide · sulfoxyl · NSC-8400
Score:
#1022 in Biochemistry
,
#2669 in Biology
,
#3336 in Chemistry
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- A Rapid Permethylation of Glycolipid, and Polysaccharide Catalyzed by Methylsulfinyl Carbanion in Dimethyl Sulfoxide (Journal of Biochemistry, 1964)
- Equilibrium Acidities in Dimethyl Sulfoxide Solution (Accounts of Chemical Research, 1988)
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride (Journal of Organic Chemistry, 1978)
- Terminal differentiation of human promyelocytic leukemia cells induced by dimethyl sulfoxide and other polar compounds (Proceedings of the National Academy of Sciences of the United States of America, 1978)
- Hemoglobin Synthesis in Murine Virus-Induced Leukemic Cells In Vitro: Stimulation of Erythroid Differentiation by Dimethyl Sulfoxide (Proceedings of the National Academy of Sciences of the United States of America, 1971)
- Oxidation of alcohols by activated dimethyl sulfoxide. a preparative, steric and mechanistic study (Tetrahedron, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - sulphoxide
- sulfoxyl
- NSC-8400
- sulfoxide, (R*,R*)-isomer
- 1,2-(methylenedioxy)-4-(2-(octylsulfinyl)propyl)benzene
- piperonyl sulfoxide
- isosafrole octyl sulfoxide
- sulfox-cide
- sulfoxide, (R*,S*)-isomer
-
SMILESCCCCCCCCS(=O)C(C)CC1=CC2=C(C=C1)OCO2
-
InChIKeyATTZFSUZZUNHBP-UHFFFAOYSA-N
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