1350663-38-5

Basic information

• Product Name: 2-pyridinyl 4-methoxylphenyl selenide
• Synonyms: 2-pyridinyl 4-methoxylphenyl selenide
• CAS NO: 1350663-38-5
• Molecular Weight: 264.185
• Mol File: 1350663-38-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-pyridinyl 4-methoxylphenyl selenide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-pyridinyl 4-methoxylphenyl selenide(1350663-38-5)
• EPA Substance Registry System: 2-pyridinyl 4-methoxylphenyl selenide(1350663-38-5)

Safety Data

• Hazardous Substances Data: 1350663-38-5(Hazardous Substances Data)

Upstream product

• 109-04-6 2-bromo-pyridine 
• 38762-70-8 bis(4-methoxyphenyl)diselenide 
• 59957-75-4 2,2'-dipyridyldiselenide 
• 5720-07-0 4-methoxyphenylboronic acid 
• 109-09-1 2-chloropyridine 
• 82998-10-5 2-pyridineselenenyl chloride 

Relevant articles and documents

An electrochemical method for deborylative selenylation of arylboronic acids under metal- and oxidant-free conditions

An efficient protocol to synthesize aryl selenoethers through deborylative selenylation of widely available arylboronic acids has been established under electrochemical conditions in the absence of metal catalyst and external oxidant. The synthesis of bio

Silver-Catalyzed Synthesis of Diaryl Selenides by Reaction of Diaryl Diselenides with Aryl Boronic Acids

We described herein our results on the silver-catalyzed synthesis of diaryl selenides via a cross-coupling reaction of diaryl diselenides with aryl boronic acids. The methodology is tolerant to electron-donor and electron-withdrawing groups at the substrates and the desired products were obtained in good to excellent yields.

Synthesis of diaryl selenides using electrophilic selenium species and nucleophilic boron reagents in ionic liquids

We described herein the use of imidazolium ionic liquids [bmim]PF 6 and [bmim]BF4 in the selective, metal and catalyst-free synthesis of unsymmetrical diaryl selenides by electrophilic substitution in arylboron reagents with arylselenium halides (Cl and Br) at room temperature. This is a general substitution reaction and it was performed with arylboronic acids or potassium aryltrifluoroborates bearing electron-withdrawing or electron-donating groups, affording the corresponding diaryl selenides in good to excellent yields. The ionic liquid [bmim][PF6] was easily recovered and utilized for further substitution reactions.