181143-79-3

Basic information

• Product Name: 2-hydroxybutyl phenyl selenide
• Synonyms: 2-hydroxybutyl phenyl selenide
• CAS NO: 181143-79-3
• Molecular Weight: 229.181
• Mol File: 181143-79-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-hydroxybutyl phenyl selenide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxybutyl phenyl selenide(181143-79-3)
• EPA Substance Registry System: 2-hydroxybutyl phenyl selenide(181143-79-3)

Safety Data

• Hazardous Substances Data: 181143-79-3(Hazardous Substances Data)

Upstream product

• 106-88-7 ethyloxirane 
• 98-80-6 phenylboronic acid 
• 591-50-4 iodobenzene 
• 30095-63-7 2-ethyl-2-methyloxirane 
• 1666-13-3 diphenyl diselenide 

Relevant articles and documents

Silver-Catalyzed One-Pot Three-Component Selective Synthesis of β-Hydroxy Selenides

A convenient, multi-component reaction of organoboronic acids, selenium powder and epoxides has been developed, providing an efficient protocol for the synthesis of β-hydroxy selenides with excellent selectivity and good functional group tolerance. Preliminary mechanistic studies suggest that the reaction proceeds through the silver-catalyzed radical selenation of the arylboronic acids to generate a diselenide, and subsequent selenium-mediated selective ring-opening arylselenation of epoxides. (Figure presented.).

A β- hydroxyl selenium etheration method for synthesizing compound of

The invention relates to a synthetic method of Beta-hydroxyl selenide compound. The method includes: in organic solvent, in the presence of catalyst and alkali, allowing halogenated compound to react with elemental Se and epoxy compound to obtain Beta-hydroxyl selenide compound. The synthetic method has the advantages that reaction is simple, operating is simple, yield is high, the method is a novel one, a novel synthetic route is provided for the synthesis of the Beta-hydroxyl selenide compounds, and the method has good scientific research value and industrial potential.

Convenient preparation of ytterbium(III) chalcogenolate complexes by insertion of ytterbium into chalcogen-chalcogen bonds. Application in the ring-opening of epoxides

Convenient conditions are reported for the preparation of ytterbium(III) chalcogenolate complexes by insertion of ytterbium metal into the chalcogen- chalcogen bond of disulfides, diselenides, and ditellurides. The resulting complexes have been found to t