68090-01-7

Upstream product

• 620-22-4 3-Methylbenzonitrile 

Downstream Products

• 68723-59-1 3,5-di-m-tolyl-[1,2,4]selenadiazole 
• 38572-14-4 bis(benzoyl) selenide 
• 620-22-4 3-Methylbenzonitrile 
• 65212-15-9 bis(4-methoxybenzoic) selenoanhydride 
• 75103-25-2 2-m-tolyl-selenazole-4-carbaldehyde 
• 75103-19-4 (2-m-tolyl-selenazol-4-yl)-methanol 
• 75103-31-0 2-azido-3-(2-m-tolyl-selenazol-4-yl)-acrylic acid ethyl ester 
• 75103-37-6 2-m-tolyl-4H-pyrrolo[3,2-d]selenazole-5-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

A synthetic and structural study of arylselenoamides and 2,4-diaryl-1,3- selenazoles

The systematic preparation of 2,4-diaryl-1,3-selenazoles was carried out by two-component cyclization of the primary selenoamides with α-halo ketones. Selenoamides were obtained from the reaction of Woollins' reagent with arylnitrile, followed by hydrolys

Synthesis of primary arylselenoamides by reaction of aryl nitriles with Woollins' reagent

The reaction of aryl nitriles with Woollins' reagent followed by water affords a variety of primary arylselenoamides In 60-100% yield. The first crystal structures of two primary selenoamides are reported.

Convenient synthesis of primary selenoamides from aryl nitriles, selenium and sodium borohydride

Aryl nitriles react smoothly with sodium hydrogen selenide, itself prepared in situ from selenium and sodium borohydride, in ethanol to give the corresponding primary selenoamides in moderate to good yield.