588676-13-5 Usage
Chemical Class
2-(2,4-Difluorophenoxy)acetohydrazide belongs to the class of acetohydrazides.
Synthesis
It is synthesized by reacting 2,4-difluorophenoxyacetyl chloride with hydrazine.
Pharmaceutical Applications
It has various applications in the pharmaceutical industry, including as a building block in the synthesis of biologically active compounds.
Agricultural Applications
It is used in the agricultural industry as an intermediate in the production of herbicides.
Antifungal Properties
2-(2,4-Difluorophenoxy)acetohydrazide has potential antifungal properties and is being researched for its potential use in medicinal products.
Antibacterial Properties
It also has potential antibacterial properties and is being studied for its potential use in the development of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 588676-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,8,6,7 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 588676-13:
(8*5)+(7*8)+(6*8)+(5*6)+(4*7)+(3*6)+(2*1)+(1*3)=225
225 % 10 = 5
So 588676-13-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H8F2N2O2/c9-5-1-2-7(6(10)3-5)14-4-8(13)12-11/h1-3H,4,11H2,(H,12,13)
588676-13-5Relevant academic research and scientific papers
Synthesis and larvicidal activity of 1,3,4-oxadiazole derivatives containing a 3-chloropyridin-2-yl-1H-pyrazole scaffold
Wang, Yanyan,Lu, Xiumian,Shi, Jun,Xu, Jiahong,Wang, Fenghua,Yang, Xiao,Yu, Gang,Liu, Zhiqian,Li, Chuanhui,Dai, Ali,Zhao, Yonghui,Wu, Jian
, p. 611 - 623 (2018/01/17)
Abstract: A new series of 1,3,4-oxadiazole derivatives with a 3-chloropyridin-2-yl-1H-pyrazole moiety was designed, synthesized, and characterized. The results of bioassay against Helicoverpa armigera and Plutella xylostella indicated that some of the synthesized compounds showed remarkable larvicidal activity. In particular, the LC50 values of the most active compounds against P. xylostella were 46.5, 23.9, and 13.9?mg/dm3, and against Helicoverpa armigera were 88.3 and 69.5?mg/dm3, the latter being slightly better than commercial chlorpyrifos (LC50 103.77?mg/dm3). Preliminary SAR was also discussed. Graphical abstract: [Figure not available: see fulltext.].
