877315-80-5

Upstream product

• 877315-76-9 ethyl o-chlorophenylacetate ethoxycarbonyl hydrazone 
• 55770-05-3 ethyl o-chlorophenylimidoacetate hydrochloride 
• 2856-63-5 2-Chlorophenylacetonitrile 

Downstream Products

• 1174660-13-9 4-(3-bromobenzylideneamino)-3-(2-chlorobenzyl)-4,5-dihydro-1H-1,2,4-triazol-5-one 
• 1174660-09-3 4-(4-tert-butylbenzylideneamino)-3-(2-chlorobenzyl)-4,5-dihydro-1H-1,2,4-triazol-5-one 
• 1174660-11-7 3-(2-chlorobenzyl)-4-(4-chlorobenzylideneamino)-4,5-dihydro-1H-1,2,4-triazol-5-one 
• 1174660-17-3 3-(2-chlorobenzyl)-4-(3,4,5-trimethoxybenzylideneamino)-4,5-dihydro-1H-1,2,4-triazol-5-one 
• 1174660-05-9 4-benzylideneamino-3-(2-chlorobenzyl)-4,5-dihydro-1H-1,2,4-triazol-5-one 
• 1470364-71-6 5-(o-chlorobenzyl)-4-m-chlorobenzyliden amino-2,4-dihydro-2H-1,2,4-triazol-3-one 
• 1470364-72-7 5-(o-chlorobenzyl)-4-m-bromo-4-fluorobenzyliden amino-2,4-dihydro-2H-1,2,4-triazol-3-one 
• 1470364-73-8 5-(o-chlorobenzyl)-4-p-nitrobenzyliden amino-2,4-dihydro-2H-1,2,4-triazol-3-one 

Relevant academic research and scientific papers

Microwave-assisted synthesis of some new benzylidenamino compounds and potentiometric determination of their pKa

A growing body of literature has shown the effectiveness of using microwaves in chemical reactions. The aim of this study is to demonstrate a rapid and highly efficient synthesis of some new benzylidenamino compounds (4a-f) via microwave heating using a m

Microwave-assisted synthesis and antifungal activity of some new 1H-1,2,4-triazole derivatives

A number of 3-aryl-4-arylmethylideneamino-4,5-dihydro-1H-1,2,4-triazol-5- ones were synthesized by reaction of the corresponding aromatic aldehydes with 4-amino-3-aryl-1H-1,2,4-triazol-5-ones in anhydrous ethanol under microwave irradiation. The newly synthesized 1H-1,2,4-triazole derivatives were tested for antimicrobial activity. They showed no antibacterial activity but slight mycostatic activity against some Candida species.

Synthesis of 4-amino-4,5-dihydro-1H-1,2,4-triazole-5-ones and their isatin-3-imine derivatives

Iminoester hydrochlorides 1 have been synthesized. These compounds were then converted into ester ethoxycarbonyl hydrazones 2, from which in turn a new series of substituted 4-amino-4,5-dihydro-1H-1,2,4-triazole-5-ones, 3, was then prepared. Finally a set