| Weight | 312.132 g/mol |
|---|---|
| Formula | C12H10Se2 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
Diphenyl diselenide (1666-13-3)
diphenyldiselenide
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#1190 in Neuroscience
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#5125 in Biology
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#6663 in Chemistry
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- Sigma-Aldrich - Diphenyl diselenide54.80 - 478.50 USD
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- TCI - Diphenyl diselenide47.00 - 129.00 USD
- Diphenyl diselenide and ascorbic acid changes deposition of selenium and ascorbic acid in liver and brain of mice. (Pharmacology & Toxicology, 2001)
- Anti-inflammatory and antinociceptive activity of diphenyl diselenide. (Inflammation Research, 2003)
- Diphenyl diselenide and diphenyl ditelluride differentially affect -aminolevulinate dehydratase from liver, kidney, and brain of mice (Journal of Biochemical and Molecular Toxicology, 2000)
- Potential renal and hepatic toxicity of diphenyl diselenide, diphenyl ditelluride and Ebselen for rats and mice (Toxicology Letters, 2003)
- Diphenyl diselenide a janus-faced molecule (Journal of the Brazilian Chemical Society, 2010)
- Diphenyl diselenide and diphenyl ditelluride affect the rat glutamatergic system in vitro and in vivo. (Brain Research, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - diphenyldiselenide
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SMILESC1=CC=C(C=C1)[Se][Se]C2=CC=CC=C2
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InChIKeyYWWZCHLUQSHMCL-UHFFFAOYSA-N
- Pubchem - Diphenyl diselenide
- Wikipedia - Diphenyl diselenide
Diphenyl diselenide is the chemical compound with the formula (C6H5)2Se2, abbreviated Ph2Se2 This orange-coloured solid is the oxidized derivative of benzeneselenol. It is used as a source of the PhSe unit in organic synthesis. Ph2Se2 is prepared by the oxidation of benzeneselenoate, the conjugate base of benzeneselenol which is generated via the Grignard reagent: PhMgBr + Se PhSeMgBr 2 PhSeMgBr + Br2 Ph2Se2 + 2 MgBr2 The molecule has idealized C2-symmetry, like hydrogen peroxide and related molecules.
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Diphenyl diselenide
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