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Diphenyl diselenide

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Diphenyl diselenide Basic information

Product Name:
Diphenyl diselenide
Synonyms:
  • DIPHENYL DISELENIDE FOR SYNTHESIS
  • Two phenyltwo se
  • Diphenyl diselenide purum, >=97.0% (GC)
  • PHENYL DISELENIDE
  • 1,2-Diphenyldiselane
  • Bis(phenylselenide)
  • diphenyl-diselenid
  • Diselenide,diphenyl
CAS:
1666-13-3
MF:
C12H10Se2
MW:
312.13
EINECS:
216-780-2
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Aromatic Phenylacetic Acids and Derivatives
  • organoselenides
  • Organic Building Blocks
  • Selenium Compounds
  • Pharmaceutical Intermediates
  • Classes of Metal Compounds
  • Se (Selenium) Compounds
  • Semimetal Compounds
Mol File:
1666-13-3.mol
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Diphenyl diselenide Chemical Properties

Melting point:
60 °C
Boiling point:
202 °C / 11mmHg
Density 
1.5570
refractive index 
1.7430
storage temp. 
Store below +30°C.
form 
Powder
color 
yellow
Specific Gravity
1.84
Water Solubility 
Insoluble
Hydrolytic Sensitivity
8: reacts rapidly with moisture, water, protic solvents
BRN 
2047179
Exposure limits
ACGIH: TWA 0.2 mg/m3
NIOSH: IDLH 1 mg/m3; TWA 0.2 mg/m3
CAS DataBase Reference
1666-13-3(CAS DataBase Reference)
NIST Chemistry Reference
Diselenide, diphenyl(1666-13-3)
EPA Substance Registry System
Diselenide, diphenyl (1666-13-3)
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Safety Information

Hazard Codes 
T,N
Risk Statements 
23/25-33-50/53
Safety Statements 
20/21-28-45-60-61-28A
RIDADR 
UN 3283 6.1/PG 2
WGK Germany 
3
RTECS 
JM9152500
TSCA 
Yes
HS Code 
2931 90 00
HazardClass 
6.1
PackingGroup 
II

MSDS

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Diphenyl diselenide Usage And Synthesis

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.]

Diphenyl diselenide Preparation Products And Raw materials

Raw materials

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