65169-45-1 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-5-Methyl-nicotinaMide is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-5-Methyl-nicotinaMide serves as an intermediate for the production of agrochemicals. Its incorporation into these compounds can contribute to the development of effective pesticides, herbicides, and other agricultural products that enhance crop protection and yield.
Used in Organic Electronics:
2-Chloro-5-Methyl-nicotinaMide also has potential applications in the field of organic electronics. Its unique properties may be harnessed in the development of organic semiconductors, which are crucial for creating flexible and cost-effective electronic devices such as solar cells, displays, and sensors.
It is important to handle 2-Chloro-5-Methyl-nicotinaMide with care and follow proper safety protocols when working with this chemical, given its reactivity and potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 65169-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,6 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65169-45:
(7*6)+(6*5)+(5*1)+(4*6)+(3*9)+(2*4)+(1*5)=141
141 % 10 = 1
So 65169-45-1 is a valid CAS Registry Number.
65169-45-1Relevant academic research and scientific papers
Methyl, trifluoromethyl, and methoxycarbonyl - Introduction to the fifth position on the pyridine ring of chloronicotinyl insecticide imidacloprid
Kagabu, Shinzo
, p. 1235 - 1245 (2007/10/03)
Imidacloprid is the first chloronicotinyl insecticide and is currently the largest-selling insecticide worldwide. As a project to find its variants of different insecticidal spectra, derivatives substituted with methyl, trifluoromethyl, and methoxy-carbonyl at the fifth position on the pyridine ring of imidacloprid were prepared. Copyright Taylor & Francis Group, LLC.
