27892-74-6

Upstream product

• 3352-98-5 p-methyl acetophenone semicarbazone 
• 122-00-9 para-methylacetophenone 
• 120445-91-2 1-p-tolyl-ethanone-E-semicarbazone 

Downstream Products

• 102104-53-0 2-p-Tolylethynylselanylmethyl-oxirane 
• 102104-57-4 1,3-Bis-p-tolylethynylselanyl-propan-2-ol 
• 168699-88-5 2-(p-methylbenzylidene)-4-(p-tolyl)-1,3-diselenol 
• 107406-46-2 1-Phenyl-2-p-tolylethynylselanyl-ethanone 
• 81888-37-1 1-Methyl-4-methylselanylethynyl-benzene 
• 65456-32-8 5-p-Tolyl-[1,3]thiaselenole-2-thione 
• 127901-81-9 Phenyl-[4-p-tolyl-[1,3]diselenol-(2Z)-ylidene]-amine 
• 93515-72-1 N-[5-p-Tolyl-[1,3]thiaselenol-(2E)-ylidene]-acetamide 
• 93515-70-9 N-[5-p-Tolyl-[1,3]thiaselenol-(2E)-ylidene]-benzamide 
• 74277-56-8 [5-p-Tolyl-[1,3]thiaselenol-(2Z)-ylidene]-carbamic acid ethyl ester 
• 65299-38-9 Potassium; p-tolyl-ethyneselenolate 
• 93515-71-0 4-Methyl-N-[5-p-tolyl-[1,3]thiaselenol-(2E)-ylidene]-benzamide 

Relevant academic research and scientific papers

Preparation of 2-Arylethynylselanylacetonitriles from 4-Aryl-1,2,3-selenadiazoles

Base decomposition of 4-(substituted phenyl)-1,2,3-selenadiazoles at room temperature resulted in 2-(substituted phenyl)-ethynylselenolate anions, which were immediately reacted with bromoacetonitrile to give a series of 2-(substituted phenyl)ethynylselan