248255-70-1 Usage
Uses
Used in Pharmaceutical Synthesis:
5-Chloro-3-fluoro-2-hydrazinylpyridine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into drug molecules targeting specific biological pathways. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Development:
In the agrochemical industry, 5-chloro-3-fluoro-2-hydrazinylpyridine is utilized as a building block for the creation of new agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Antimicrobial Applications:
5-Chloro-3-fluoro-2-hydrazinylpyridine has been studied for its potential antimicrobial activities, making it a candidate for use as an antimicrobial agent in various applications where resistance to existing treatments is a concern.
Used in Antitumor Research:
5-chloro-3-fluoro-2-hydrazinylpyridine has also shown promise in antitumor activities, indicating its potential use in oncology research and development for the creation of novel anti-cancer drugs.
Overall, 5-chloro-3-fluoro-2-hydrazinylpyridine is a chemical entity with broad potential across medicine and agriculture, offering a foundation for innovation in treatment and protection solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 248255-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,8,2,5 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 248255-70:
(8*2)+(7*4)+(6*8)+(5*2)+(4*5)+(3*5)+(2*7)+(1*0)=151
151 % 10 = 1
So 248255-70-1 is a valid CAS Registry Number.
248255-70-1Relevant academic research and scientific papers
IMIDAZOLE AND TRIAZOLE CONTAINING BICYCLIC COMPOUNDS AS JAK INHIBITORS
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Paragraph 0272-0273, (2020/08/05)
The invention provides compounds of formula (I): or a pharmaceutically-acceptable salt thereof, wherein the variables are defined in the specification, that are inhibitors of JAK kinases, particularly JAK3. The invention also provides pharmaceutical compo
Process for preparing 2-aminopyridine derivatives
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Page/Page column 3-4, (2008/06/13)
A method for preparing 2-aminopyridine derivatives, which comprises substituting of fluorine for hydrazine moiety and reducing with hydrogen using 3-substituted-2,5,6-trifluoropyridine as a starting material, provides 2-aminopyridine derivatives having a purity over 98% under a mild reaction condition.
Removal of fluorine from and introduction of fluorine into polyhalopyridines: An exercise in nucleophilic hetarenic substitution
Bobbio, Carla,Rausis, Thierry,Schlosser, Manfred
, p. 1903 - 1910 (2007/10/03)
Starting from six industrially available fluorinated pyridines, an expedient access to all three tetrafluoropyridines (2-4), all six trifluoropyridines (5-10), and the five non-commercial difluoropyridines (11-14 and 16) was developed. The methods employed for the selective removal of fluorine from polyfluoropyridines were the reduction by metals or complex hydrides and the site-selective replacement by hydrazine followed by dehydrogenation-dediazotation or dehydrochlorination-dediazotation. To introduce an extra fluorine atom, a suitable precursor was metalated and chlorinated before being subjected to a chlorine/ fluorine displacement process.
