696-42-4 Usage
Uses
Used in Pharmaceutical Drug Development:
3-Cyano-5-Fluoropyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence in the molecular structure can influence the properties and efficacy of the final drug product, making it an essential component in the development of new medications.
Used in Organic Synthesis:
In the field of organic chemistry, 3-Cyano-5-Fluoropyridine serves as a versatile building block for the creation of more complex molecules. Its active functional groups allow for a range of chemical reactions, facilitating the synthesis of a wide array of organic compounds for various applications, including materials science, agrochemicals, and specialty chemicals.
Used in Research and Development:
3-Cyano-5-Fluoropyridine is also utilized in academic and industrial research settings to explore its potential applications and properties. Scientists and researchers use 3-CYANO-5-FLUOROPYRIDINE to investigate its reactivity, stability, and interactions with other molecules, which can lead to the discovery of new chemical processes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 696-42-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 696-42:
(5*6)+(4*9)+(3*6)+(2*4)+(1*2)=94
94 % 10 = 4
So 696-42-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3FN2/c7-6-1-5(2-8)3-9-4-6/h1,3-4H
696-42-4Relevant academic research and scientific papers
INDOLE AHR INHIBITORS AND USES THEREOF
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, (2018/11/22)
The present invention provides compounds useful as inhibitors of AHR, compositions thereof, and methods of using the same.
Pd-catalyzed nucleophilic fluorination of aryl bromides
Lee, Hong Geun,Milner, Phillip J.,Buchwald, Stephen L.
supporting information, p. 3792 - 3795 (2014/04/03)
On the basis of mechanism-driven reaction design, a Pd-catalyzed nucleophilic fluorination of aryl bromides and iodides has been developed. The method exhibits a broad substrate scope, especially with respect to nitrogen-containing heteroaryl bromides, and proceeds with minimal formation of the corresponding reduction products. A facilitated ligand modification process was shown to be critical to the success of the reaction.
TRIAZOLOPYRIDYL COMPOUNDS AS ALDOSTERONE SYNTHASE INHIBITORS
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Page/Page column 37, (2013/04/10)
This invention relates to triazolopyridyl compounds of the structural formula: [Formula should be inserted here] or their pharmaceutically acceptable salts, wherein the variable are defined herein. The inventive compounds selectively inhibit aldosterone synthase. This invention also provides for pharmaceutical compositions comprising the compounds of Formula I or their salts as well as potentially to methods for the treatment, amelioration or prevention of conditions that could be treated by inhibiting aldosterone synthase.
