162969-65-5 Usage
Chemical class
Oxadiazole It belongs to the oxadiazole class of compounds, which are known for their diverse range of applications in various fields.
N-hydroxy derivative
5-methyl-1,2,4-oxadiazole-3-carboximidamide This compound is an N-hydroxy derivative of 5-methyl-1,2,4-oxadiazole-3-carboximidamide, which is a key structural feature.
Pharmaceutical and agrochemical development
Commonly used The compound is commonly used in the development of pharmaceuticals and agrochemicals due to its unique properties.
Agricultural industry uses
Pesticide or herbicide The compound may also have uses in the agricultural industry as a pesticide or herbicide, indicating its potential for controlling pests and unwanted plant growth.
Unique chemical structure
Attracts interest The compound's unique chemical structure has attracted interest from researchers and scientists, making it a valuable compound for further research and development.
Potential biological activities
Valuable for research The compound's potential biological activities make it a promising candidate for the development of new drugs and other applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 162969-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,6 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 162969-65:
(8*1)+(7*6)+(6*2)+(5*9)+(4*6)+(3*9)+(2*6)+(1*5)=175
175 % 10 = 5
So 162969-65-5 is a valid CAS Registry Number.
162969-65-5Relevant articles and documents
Synthesis and properties of gem-dinitro energetic salts based on 1,2,4-oxadiazole with low impact sensitivity
Lu, Tian,He, Yuna,Song, Jia,Hou, Zhengwen,Yin, Hongquan,Fan, Guijuan,Chen, Fu-Xue
, p. 526 - 529 (2021)
Eight energetic salts with a gem-dinitro group based on 1,2,4-oxadiazole were developed. All of the structures were confirmed by infrared (IR) spectroscopy, 1H and 13C nuclear magnetic resonance (NMR) spectroscopy, and high-resolution mass spectrometry (HRMS), and single-crystal X-ray diffraction was used to determine the structures of the pivotal intermediate 3-(chlorodinitromethyl)-5-methyl-1,2,4-oxadiazole (3), the potassium salt (4) and the hydrazinium salt (7). All of them are insensitive to impact (>40 J) and have higher energy levels than trinitrotoluene (TNT). This journal is
