817568-86-8 Usage
Type of compound
Oxadiazole amine
This classifies the compound as a derivative of oxadiazole, which is a five-membered ring containing two nitrogen atoms and one oxygen atom.
Substitution
1,2,4-Triazol-3-yl methyl
The compound has a 1,2,4-triazol-3-yl methyl group attached to it, which is a five-membered ring containing three nitrogen atoms and one methyl group.
Potential applications
Pharmaceutical, agrochemical, and organic synthesis
The compound can be used as a building block for the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and functional groups.
Presence of functional groups
Oxadiazole and triazolyl
The molecule contains both oxadiazole and triazolyl groups, which may have potential applications in medicinal chemistry.
Target
Biological pathways and processes
The compound may be useful in the development of new drugs targeting various biological pathways and processes due to its unique structure and functional groups.
Further research
Warranted
More research and exploration of the compound's properties and potential applications are needed to fully understand its utility in chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 817568-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,5,6 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 817568-86:
(8*8)+(7*1)+(6*7)+(5*5)+(4*6)+(3*8)+(2*8)+(1*6)=208
208 % 10 = 8
So 817568-86-8 is a valid CAS Registry Number.
817568-86-8Relevant academic research and scientific papers
Al-Soud, Yaseen A.,Al-Dweri, Mohammad N.,Al-Masoudi, Najim A.
, p. 775 - 783 (2004)
A series of 1,5-dialkyl-1,2,4-triazole derivatives of acetic acid alkylidene hydrazides 8-12, the acid 13, 1,5-dialkyl-3-(5-mercapto-4-N-aryl-1H- [1,2,4]-triazol-3-ylmethylene)-1H-[1,2,4] triazoles 14-16, their 1,3,4-oxadiazole analogues 17-21, as well as the 1,2,4-triazolo-indoles 25 and 27 were prepared. The Z/E conformations of some acetic acid alkylidene derivatives were studied by NMR spectroscopy. Most of the target compounds were evaluated in a series of human cancer cell in cultures and none have shown activity except 25 which exhibited remarkable activity against nine cancer types. No in vitro antiviral activity against HIV-1, HIV-2, HSV-1, HSV-2, SV, CV-B4, RSV, P3V, RV, SinV, PTV has been found for all the synthesized compounds.
