770732-47-3

Upstream product

• 56559-63-8 1-benzyl-1H-indole-3-carbohydrazide 
• 155134-26-2 1-Benzyl-1H-indole-3-carboxylic acid methyl ester 
• 100-39-0 benzyl bromide 
• 942-24-5 3-methoxycarbonylindole 
• 776-41-0 indole-3-carboxylic acid ethyl ester 
• 770732-44-0 2-(1-benzyl-1H-indol-3-yl)-1,3,4-oxadiazole-5(4H)-thione 
• 100-44-7 benzyl chloride 
• 56559-61-6 ethyl 1-benzyl-1H-indole-3-carboxylate 

Downstream Products

• 1392495-67-8 C₃₆H₃₂N₁₀S₂ 
• 1392495-72-5 C₅₀H₄₀N₁₀O₂S₂ 
• 1392495-73-6 C₅₀H₃₈Br₂N₁₀S₂ 
• 1392495-74-7 C₅₀H₃₈N₁₂O₄S₂ 
• 1392495-75-8 C₅₀H₃₈Br₂N₁₀S₂ 
• 1392495-76-9 C₅₀H₃₈Br₂N₁₀S₂ 
• 1392495-77-0 C₄₆H₃₆N₁₀O₂S₂ 
• 1392495-68-9 C₅₀H₄₀N₁₀S₂ 
• 1392495-69-0 C₅₀H₃₈F₂N₁₀S₂ 
• 1392495-70-3 C₅₀H₄₀N₁₀O₂S₂ 

Relevant academic research and scientific papers

Microwave-assisted synthesis and biological activity of new Schiff bases derived from dimers of 4-amino-3-[3-(1-benzyl)indole]-5-thiomethyl-1,2,4- triazole

An expeditious method with microwave irradiation has been developed for synthesis of novel Schiff bases from dimers of 4-amino-3-[3-(1-benzyl)indole]-5- thiomethyl-1,2,4-triazole. Its distinct advantages are short reaction times and good conversion. The s

Synthesis, reactions and antimicrobial activity of some new indolyl-1,3,4-oxadiazole, triazole and pyrazole derivatives

Indole-3-carboxylic acid hydrazide 3 was prepared and was treated with aromatic aldehydes in ethanol to give the corresponding hydrazone derivatives 4-7 in good yields. The indole carbohydrazide was incorporated into the 3-indolyloxadiazoles 8-11 and 18, 3-indolyltriazoles 13-17 and 35, 3-indolylpyrazole derivatives 19-23 and carbamate derivatives 26-27. Furthermore, interaction of the carboazide 24 with hydrazine hydrate in refluxing toluene afforded the corresponding semicarbazide derivative 30. The thiadiazine derivative 34 was also prepared. Some of these compounds were screened in vitro for their antibacterial and antifungal activity.