Dibenzyl diselenide

Dibenzyl diselenide Basic information
Product Name:Dibenzyl diselenide
Synonyms:BENZYL DISELENIDE;DIBENZYL DISELENIDE;1,2-Dibenzyldiselane;Dibenzyldiselenium;Diselenide,bis(phenylmethyl);Dibenzyldiselenide, 99+%;Bis(benzyl) perselenide;Dibenzyl perdiselenide
CAS:1482-82-2
MF:C14H14Se2
MW:340.18
EINECS:
Product Categories:Pharmaceutical Intermediates;Classes of Metal Compounds;Se (Selenium) Compounds;Semimetal Compounds;Building Blocks;Organic Building Blocks;Selenium Compounds
Mol File:1482-82-2.mol
Dibenzyl diselenide Structure
Dibenzyl diselenide Chemical Properties
Melting point 91-93 °C(lit.)
Boiling point 427.3±48.0 °C(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility almost transparency in hot Toluene
form solid
color Light yellow to Yellow to Orange
Water Solubility Soluble in water.
Sensitive Air Sensitive
BRN 1877745
Exposure limitsACGIH: TWA 0.2 mg/m3
NIOSH: IDLH 1 mg/m3; TWA 0.2 mg/m3
InChIKeyHYAVEDMFTNAZQE-UHFFFAOYSA-N
CAS DataBase Reference1482-82-2(CAS DataBase Reference)
NIST Chemistry ReferenceDiselenide, bis(phenylmethyl)(1482-82-2)
Safety Information
Hazard Codes T,N
Risk Statements 23/25-33-50/53
Safety Statements 20/21-28-45-60-61
RIDADR UN 3283 6.1/PG 2
WGK Germany 3
HazardClass 6.1
PackingGroup III
HS Code 29310099
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
Dibenzyl diselenide Usage And Synthesis
Chemical PropertiesLight yellow to Yellow to Orange powder to crystaline.
UsesDibenzyl diselenide is used as a source of the PhSe unit in organic synthesis. It is also used to introduce PhSe groups by reaction with a variety of nucleophilic, including enolates, enol silyl ethers, Grignard reagents, organolithium reagents, alkenes and amines.
PreparationDibenzyl diselenide was synthesized from bis(methoxymagnesium) diselenide reagent as reported by Gunther using benzyl chloride (6.3 g, 0.05 mole) and a methanolic solution of bis(methoxymagnesium) diselenide reagent (from 0.05 gatom of selenium). After 10 min stirring, water (100 mL) and concentrated hydrochloric acid (5 mL) were added, the solution was cooled, and the black solid was collected by filtration. This black solid was then extracted with ethanol to yield a bright yellow solution which, upon solvent removal, gave a yellow crystalline product. The 1H NMR of the yellow solid (in CDCl3) was identical to that of commercially available dibenzyl diselenide.
Dibenzyl diselenide Preparation Products And Raw materials
Raw materialsBenzyl chloride-->N,N-Dimethylformamide-->Benzaldehyde-->Selenium-->Diethyl ether-->Sodium hydroxide
Dimethyldiselenide DIPHENYL DISULFIDE ZINC TELLURIDE p-Toluenethiol Dibenzyl diselenide Dimethylbenzylcarbinyl acetate Selenium Benzyltriethylammonium chloride DIETHYLDISELENIDE Diphenyl ether Diethylene glycol monobutyl ether Dimethyl sulfide HYDROGEN SELENIDE Triclosan methaneselenol Dimethyl disulfide DIBENZYLTOLUENE

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