70231-34-4

Upstream product

• 70231-39-9 5,5-dimethyl-3-(1-phenylvinyl)-4-(1-pyrrolidinyl)-Δ¹-1,2,3-triazoline 

Downstream Products

• 70231-35-5 dimethyl 2-isopropyl-6-phenylpyridine-3,4-dicarboxylate 
• 10413-00-0 5-oxo-5-phenylpentanenitrile 
• 70231-36-6 3-cyano-2-isopropyl-6-phenylpyridine 
• 70231-37-7 3-cyano-1,4-dihydro-2-isopropyl-6-phenylpyridine 
• 80541-55-5 3-cyano-5-(2-cyanoethyl)-2-isopropyl-6-phenylpyridine 
• 80541-57-7 2-isopropyl-6-phenylnicotinaldehyde 
• 80541-56-6 1,4-dihydro-2-isopropyl-6-phenylnicotinaldehyde 
• 70231-38-8 methyl 2-isopropyl-6-phenylnicotinate 
• 80541-58-8 methyl 2-isobutyryl-5-oxo-5-phenylpentanoate 

Relevant academic research and scientific papers

Acid Decomposition of 5-Amino-1-vinyl-4,5-dihydro-1H-1,2,3-triazoles. A Novel Formation of 1-Amino-2-azabutadienes

Acid decomposition of 4-alkyl-5-dialkyl-amino-1-vinyl-4,5-dihydro-1H-1,2,3-triazoles gave N1,N1-dialkyl-N2-vinylalkanamidines, which have 2-aza-1,3-butadiene skeleton, in fair yields.

5-Amino-1-vinyl-4,5-dihydro-1H-1,2,3-triazoles as a Source of 1-Amino-2-aza-1,3-butadiene

Thermolysis of 4,4-dimethyl-1-(1-phenylvinyl)-5-(1-pyrrolidinyl)-4,5-dihydro-1H-1,2,3-triazole gave 2-methyl-N-(1-phenylvinyl)-1-(1-pyrrolidinyl)-1-propanimine, which reacted as a 2-azabutadiene with electrondeficient dienophiles to afford the corresponding cycloadducts.Reactivity and regioselectivity of the cycloaddition reactions were rationalized with the frontier molecular orbital treatment.