112225-92-0Relevant academic research and scientific papers
Azophenylene-1-bishydrazide carboxylate compound and bactericidal composition comprising compound
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, (2017/08/28)
The invention discloses an azophenylene-1-bishydrazide carboxylate compound. The azophenylene-1-bishydrazide carboxylate compound is characterized by being represented by a general formula (I), wherein the structural formula is as shown in the specificati
Synthesis and bioactivity of N-tert-butyl-N′-acyl-5-methyl-1,2,3- thiadiazole-4-carbohydrazides
Mao, Wu Tao,Zhao, Hui,Fan, Zhi Jin,Ji, Xiao Tian,Hua, Xue Wen,Kalinina, Tatiana,Yury, Yu. Morzherin,Vasiliy, A. Bakulev
, p. 1233 - 1236,4 (2020/10/15)
A series of novel N-tert-butyl-N′-acyl-5-methyl-1,2,3-thiadiazole-4- carbohydrazides were designed and synthesized. Their structures were characterized by melting points, 1H NMR, IR, ESI-MS, and elemental analysis. The bioassay tests indicated that compound 7o exhibited excellent direct anti-TMV activity and induction activity in vivo at 50 μg/mL, which was better than that of Ninamycin and tiadinial. Our studies indicated that 1,2,3-thiadiazole was an active substructure for novel pesticide development.
Synthesis and insecticidal activity of N - Tert -Butyl- N, N ′-diacylhydrazines containing 1,2,3-thiadiazoles
Wang, Huan,Yang, Zhikun,Fan, Zhijin,Wu, Qingjun,Zhang, Youjun,Mi, Na,Wang, Shouxin,Zhang, Zhengcai,Song, Haibin,Liu, Feng
experimental part, p. 628 - 634 (2011/10/02)
N-tert-Butyl-N,N′-diacylhydrazines are nonsteroidal ecdysone agonists used as environmental benign pest regulators. In this paper, two series of new N-tert-butyl-N,N′-diacylhydrazine derivatives containing 1,2,3-thiadiazole were designed and synthesized.
Synthesis and insecticidal activity of chromanone and chromone analogues of diacylhydrazines
Zhao, Pei-Liang,Li, Jing,Yang, Guang-Fu
, p. 1888 - 1895 (2007/10/03)
Diacylhydrazine derivatives have been identified as one of the most important insect growth regulators. A variety of diacylhydrazine derivatives were designed and synthesized in recent years due to their unique action mechanism, simple structure, and environmental benign character. This paper describes the molecular design, synthesis, and insecticidal activities of a series of chromanone and chromone analogues of diacylhydrazine derivatives. The preliminary bioassay showed that some of the chromanone analogues exhibited good insecticidal activity against Mythima separata at the dosage of 500 mg L-1. The present work demonstrated that replacement of the chroman ring of ANS-118, a commercial insecticide, with chromanone moiety could result in new compounds with high potent insecticidal activity.
