94706-43-1

Basic information

• Product Name: Se-(4-methoxyphenyl) benzenecarboselenoate
• Synonyms: Se-(4-methoxyphenyl) benzenecarboselenoate
• CAS NO: 94706-43-1
• Molecular Weight: 291.208
• Mol File: 94706-43-1.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Se-(4-methoxyphenyl) benzenecarboselenoate(CAS DataBase Reference)
• NIST Chemistry Reference: Se-(4-methoxyphenyl) benzenecarboselenoate(94706-43-1)
• EPA Substance Registry System: Se-(4-methoxyphenyl) benzenecarboselenoate(94706-43-1)

Safety Data

• Hazardous Substances Data: 94706-43-1(Hazardous Substances Data)

Upstream product

• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 38762-70-8 bis(4-methoxyphenyl)diselenide 
• 93-97-0 benzoic acid anhydride 
• 65-85-0 benzoic acid 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 98-88-4 benzoyl chloride 

Downstream Products

• 895771-34-3 N-(2-aminobenzyl)benzamide 
• 80448-01-7 p-methoxyphenyl phenyl selenide 

Relevant articles and documents

Nickel-Catalyzed Intramolecular Decarbonylative Coupling of Aryl Selenol Esters

This report describes a method for Ni-catalyzed intramolecular decarbonylative coupling, which enables the conversion of areneselenol esters to diaryl selenides. The inexpensive and readily available catalyst can be employed under mild reaction conditions for the construction of structurally diverse diaryl selenides, including heterocyclic and natural product derivatives. (Figure presented.).

Synthesis of selenol esters from diorganyl diselenides and acyl chlorides under solvent-free conditions and microwave irradiation

Herein, we report an efficient, quick and eco-friendly new method for the synthesis of a variety of selenol esters. This novel solvent-free methodology gave good to excellent isolated yields of desired products after just 2 min under microwave irradiation

Ionic liquid: An efficient and reusable media for seleno- and thioester synthesis promoted by indium

A series of thio and selenoesters were efficiently obtained employing stable diorganyl chalcogenides, acyl chlorides, and In as reducing agent in BMIM·PF6. Recycling of the ionic liquid was also performed, which was reused three times.