| Identification | More | [Name]
Diphenyl diselenide | [CAS]
1666-13-3 | [Synonyms]
DIPHENYL DISELENIDE
PHENYL DISELENIDE
1,2-Diphenyldiselane
Bis(phenylselenide)
diphenyl-diselenid
Diselenide,diphenyl
diphenyl disenenide
Diphenyldiselenide,98%
1,1'-Diselenobisbenzene
Diphenyl perdiselenide
Diphenyl perselenide | [EINECS(EC#)]
216-780-2 | [Molecular Formula]
C12H10Se2 | [MDL Number]
MFCD00003001 | [Molecular Weight]
312.13 | [MOL File]
1666-13-3.mol |
| Safety Data | Back Directory | [Hazard Codes ]
T,N | [Risk Statements ]
R23/25:Toxic by inhalation and if swallowed .
R33:Danger of cumulative effects.
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S20/21:When using, do not eat, drink or smoke .
S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [RIDADR ]
UN 3283 6.1/PG 2
| [WGK Germany ]
3
| [RTECS ]
JM9152500
| [TSCA ]
Yes | [HazardClass ]
6.1 | [PackingGroup ]
II | [HS Code ]
29319090 |
| Hazard Information | Back Directory | [Chemical Properties]
yellow crystalline powder | [Uses]
Diphenyl diselenide is used in the methoxyselenenylation of alkenes, dihydroxylation of double bonds, hydrothiolation of terminal alkynes. It is used in the synthesis of the unsymmetrical diorganyl selenides, 1-(phenylselenomethyl)vinyl selenides, allylic phenyl selenides. | [General Description]
Diphenyl diselenide (Ph2Se2) is an organoselenium compound. Its crystalline structure, toxicokinetic properties, antioxidant and anti-inflammatory activities have been investigated. Its ability to reverse the oxidative brain damage and mitochondrial dysfunction induced by acetaminophen has been studied in mice. It reacts with thallium (Tl) to form TI (SePh). It participates in a four-component radical coupling to form substituted cyclopentanes. | [Biochem/physiol Actions]
Diphenyl diselenide inhibits δ-aminolevulinate dehydratase (δ-ALA-D) from brain, liver and kidney in vitro. | [Purification Methods]
Crystallise it twice from hexane [Kice & Purkiss J Org Chem 52 3448 1987]. [Beilstein 6 IV 1781.] |
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