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PHENYLSELENOL

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PHENYLSELENOL Basic information

Product Name:
PHENYLSELENOL
Synonyms:
  • SELENOPHENOL
  • PHENYLSELENOL
  • Benzene, selenyl-
  • Phenol, seleno-
  • Selenylbenzene
  • BENZENESELENOL
  • HYDROSELENOBENZENE
  • Phenylselenol,97%
CAS:
645-96-5
MF:
C6H6Se
MW:
157.07
EINECS:
211-457-2
Product Categories:
  • organoselenides
  • Selenium Compounds
  • Classes of Metal Compounds
  • Se (Selenium) Compounds
  • Semimetal Compounds
  • Building Blocks
  • Organic Building Blocks
Mol File:
645-96-5.mol
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PHENYLSELENOL Chemical Properties

Boiling point:
71-72 °C/18 mmHg (lit.)
Density 
1.479 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.616(lit.)
Flash point:
158 °F
form 
liquid
pka
4.73±0.70(Predicted)
color 
gold-yellow
Water Solubility 
Not miscible or difficult to mix in water.
Sensitive 
Air Sensitive
BRN 
385715
Exposure limits
ACGIH: TWA 0.2 mg/m3
NIOSH: IDLH 1 mg/m3; TWA 0.2 mg/m3
CAS DataBase Reference
645-96-5(CAS DataBase Reference)
EPA Substance Registry System
Benzeneselenol (645-96-5)
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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
RIDADR 
UN 2810 6.1/PG 2
WGK Germany 
3
10-23
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
II
HS Code 
29319090

MSDS

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PHENYLSELENOL Usage And Synthesis

Chemical Properties

clear yellow liquid

Uses

It is applied for reactions of phenylselenol and its anion. Benzeneselenol can used as starting reagent in the synthesis of monoseleno-substituted 1,3-dienes. It may be used in the synthesis of cationic chalcogenolato-bridged diruthenium complexes.

Uses

Benzeneselenol may be used as starting reagent in the synthesis of monoseleno-substituted 1,3-dienes. It may be used in the synthesis of cationic chalcogenolato-bridged diruthenium complexes.

General Description

Benzeneselenol is an aryl selenol. Diphenyl diselenide-promoted radical addition of benzeneselenol to inactivated acetylenes upon irradiation through Pyrex with a tungsten lamp has been reported. Catalysis of stannane-mediated radical chain reactions by benzeneselenol, generated in situ by reduction of diphenyl diselenide with tributyltin hydride, has been reported.

Purification Methods

Dissolve it in aqueous N NaOH, acidify this with conc HCl and extract with Et2O, dry over CaCl2, filter, evaporate on a steam bath and distil the residue from a Claisen flask or through a short column collecting the middle fraction, and seal immediately in a glass vial, otherwise the colourless liquid becomes yellow. The alkali insoluble materials consist of diphenylselenide (b 167o/16mm) and diphenyldiselenide, m 63o (from EtOH). TOXIC, use rubber gloves. It has a foul odour. [Foster Org Synth Coll Vol III 771 1955, Beilstein 6 III 1104, 1110, 6 IV 1777.]

PHENYLSELENOL Preparation Products And Raw materials

Raw materials

PHENYLSELENOLSupplier

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