185041-03-6 Usage
Uses
Used in Organic Synthesis:
1-(2-Chloro-4-iodopyridin-3-yl)ethanone is used as a reagent in organic synthesis for its ability to serve as a building block in the creation of other organic compounds. Its unique structure, which includes a pyridine ring with chlorine and iodine substituents, contributes to its utility in this application.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-Chloro-4-iodopyridin-3-yl)ethanone is utilized as a key component in the development of new drugs. Its properties make it a promising candidate for the synthesis of novel therapeutic agents, potentially leading to advancements in various medical fields.
Used in Material Development:
1-(2-Chloro-4-iodopyridin-3-yl)ethanone's structural features also render it useful in the development of new materials. 1-(2-Chloro-4-iodopyridin-3-yl)ethanone may contribute to the creation of innovative materials with unique properties, expanding its applications beyond the realms of organic synthesis and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 185041-03-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,0,4 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 185041-03:
(8*1)+(7*8)+(6*5)+(5*0)+(4*4)+(3*1)+(2*0)+(1*3)=116
116 % 10 = 6
So 185041-03-6 is a valid CAS Registry Number.
185041-03-6Relevant academic research and scientific papers
Synthesis of 4,5-disubstituted benzo[c][2,7]naphthyridines by combined metalation-palladium-catalysed cross-coupling strategies. Preparation of 8H-pyrido[4,3,2-mn]acridone as a model of cystodytin alkaloids
Guillier,Nivoliers,Cochennec,Godard,Marsais,Queguiner
, p. 4421 - 4436 (2007/10/03)
A short and efficient synthesis of 8H-pyrido[4,3,2-mn]acridone is described. The strategy involves the preparation of 4-chloro-5-methylbenzo[c][2,7]naphthyridine, as key intermediate, by metalation and Palladium catalyzed cross-coupling reaction. A second cross-coupling reaction and subsequent oxidation by SeO2 led to the title compound.
