68090-02-8

Upstream product

• 623-00-7 4-bromobenzenecarbonitrile 

Downstream Products

• 70250-29-2 2,5-bis(4-bromophenyl)-1,3,4-selenadiazole 
• 68723-57-9 3,5-bis(4-bromophenyl)-1,2,4-selenadiazole 
• 69625-89-4 2-(4-bromophenyl)-4-phenyl-1,3-selenazole 
• 75103-35-4 2-(4-bromo-phenyl)-4H-pyrrolo[3,2-d]selenazole-5-carboxylic acid ethyl ester 
• 75103-29-6 2-azido-3-[2-(4-bromo-phenyl)-selenazol-4-yl]-acrylic acid ethyl ester 
• 75103-17-2 [2-(4-bromo-phenyl)-selenazol-4-yl]-methanol 
• 75103-23-0 2-(4-bromo-phenyl)-selenazole-4-carbaldehyde 

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, characterization and antibacterial activity of some new ferrocenyl selenazoles and 3,5-diferrocenyl-1,2,4-selenadiazole

New ferrocenyl containing selenazole derivatives were synthesized from reactions of aryl selenocarboxamide (i.e. Ar-CSe(NH2); ArC6H5 (1), 4-Br-C6H4 (2), 4-PhC6H4 (3), 4-CH3

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.

Palladium-catalyzed formation of 3,5-diaryl-1,2,4-selenadiazoles from arylselenocarboxamide

A number of new and known arylselenocarboxamides (i.e. Ar-C(=Se)NH2; Ar=C6H5 (1), 4-BrC6H4 (2), 2-MeOC6H4 (3), 4-MeOC6H4 (4), 4-MeSC6H4/sub