160594-72-9

Basic information

• Product Name: N,N-diethyl-4-methylselenobenzamide
• Synonyms: N,N-diethyl-4-methylselenobenzamide
• CAS NO: 160594-72-9
• Molecular Weight: 254.234
• Mol File: 160594-72-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N,N-diethyl-4-methylselenobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diethyl-4-methylselenobenzamide(160594-72-9)
• EPA Substance Registry System: N,N-diethyl-4-methylselenobenzamide(160594-72-9)

Safety Data

• Hazardous Substances Data: 160594-72-9(Hazardous Substances Data)

Upstream product

• 23063-36-7 1-(dichloromethyl)-4-methylbenzene 
• 109-89-7 diethylamine 
• 2728-05-4 N,N-Diethyl-p-toluamid 

Downstream Products

• 104-87-0 4-methyl-benzaldehyde 

Relevant articles and documents

Facile synthesis of N,N-dialkylselenoamides from amides

The synthesis of the N,N-dialkylselenoamides from amides was discussed. These selenoamides were chlorinated with oxalyl chloride and then they were allowed to react with LiAlHSeH to afford the corresponding N,N-dialkylamides in moderate to good yields. Af

A Willgerodt-Kindler Type Selenation of Dihalomethane Derivatives, Chloroform, and Sodium Trichloroacetate by Treating with a Base, Elemental Selenium, and an Amine

Treatment of dihalomethane derivatives, chloroform, or sodium trichloroacetate with elemental selenium in the presence of NaH and an excess amount of an amine gave the corresponding selenoamides, selenoureas, and bis(selenocarbamoyl) triselenides in modest yields. These products were afforded from reactive intermediates related to "selenocarbonyl halides" and "selenophosgenoids" generated by the reaction of dichloromethanide ions and trichloromethanide ion with N-alkylated aminopolyselenide species (R2N-(Se)n-).