1617-92-1 Usage
General Description
5-Heptyl-[1,3,4]oxadiazol-2-ylamine is a chemical compound with the molecular formula C10H20N4O. It belongs to the oxadiazole group of compounds and consists of a seven-carbon alkyl chain attached to a 1,3,4-oxadiazole ring. 5-Heptyl-[1,3,4]oxadiazol-2-ylamine has been studied for its potential biological and pharmaceutical applications, including its antibacterial, antifungal, and antiparasitic properties. It is also being investigated for its potential use as a building block in the synthesis of novel drugs and materials. Additionally, it has shown promise as a fluorescent probe for the detection of metal ions, making it potentially useful in analytical chemistry and environmental monitoring. Further research and development of this compound may lead to a better understanding of its potential uses and benefits in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1617-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1617-92:
(6*1)+(5*6)+(4*1)+(3*7)+(2*9)+(1*2)=81
81 % 10 = 1
So 1617-92-1 is a valid CAS Registry Number.
1617-92-1Relevant articles and documents
Electrochemical synthesis of 2-amino-5-substituted-1,3,4-oxadiazole derivatives and evaluation of antibacterial activity
Kumar, Sanjeev,Pandey
, p. 252 - 258 (2013/05/09)
Some new 2-amino-5-substituted-1,3,4-oxadiazoles have been synthesized at platinum electrode through the electrochemical oxidation of semicarbazone at room temperature and studied for their antibacterial activity. This is an environmentally benign method in the field of electroorganic synthesis under controlled potential electrolysis in an undivided cell. The electrolysis have been carried out in the acetonitrile solvent and lithium perchlorate is used as a supporting electrolyte. Two platinum plates are used as working as well as counter electrode and saturated calomel electrode as the reference electrode. These compounds have been characterized by microanalyses, IR, Mass, 1H NMR and 13C NMR spectral data. All the compounds have been evaluated for their antibacterial activity against Klebsilla penumoniae, Escherichia coli, Streptococcus aureus and Shigella dysenteriea at 25 and 50 ppm concentrations.
