65169-35-9 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Chloro-3,4-dimethyl-5-nitropyridine is utilized as an intermediate in the synthesis of pharmaceuticals. Its specific chemical properties allow it to be a key component in the creation of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Production:
In addition to its pharmaceutical applications, 2-Chloro-3,4-dimethyl-5-nitropyridine also serves as an intermediate in the production of agrochemicals. Its role in this industry is crucial for the development of agricultural products that can enhance crop protection and yield.
Used as a Building Block in Organic Compounds Production:
Beyond its applications in medicine and agriculture, 2-Chloro-3,4-dimethyl-5-nitropyridine is also used as a building block in the production of other organic compounds. Its versatility in chemical reactions makes it an important precursor for synthesizing a wide range of organic molecules.
Safety Considerations:
It is important to handle 2-Chloro-3,4-dimethyl-5-nitropyridine with care due to its potential health hazards. Proper safety measures should be taken to minimize risks associated with its use in chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 65169-35-9 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, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65169-35:
(7*6)+(6*5)+(5*1)+(4*6)+(3*9)+(2*3)+(1*5)=139
139 % 10 = 9
So 65169-35-9 is a valid CAS Registry Number.
65169-35-9Relevant academic research and scientific papers
Regioselective metalation of ortho-aminopicolines using the pivaloyl group as a directing group: Synthesis of naphthyridines
Straub
, p. 365 - 372 (2007/10/02)
2-(1,3-Dioxan-2-yl)-3-methyl-4- and 2-chloro-3,4-dimethyl-5-pivaloylaminopyridines were prepared and converted to 1,6- and 1,7-naphthylpyridines via regioselective lithiation of the ortho-methyl group, reaction with 2,2-diethoxyacetophenone and subsequent
