186593-48-6 Usage
Uses
Used in Medicinal Chemistry:
2-Fluoro-3-methyl-5-aminopyridine is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic effects.
Used in Organic Synthesis:
2-Fluoro-3-methyl-5-aminopyridine is utilized as a key intermediate in organic synthesis, enabling the creation of a wide range of organic compounds with diverse applications.
Used in Material Science:
In the field of material science, 2-Fluoro-3-methyl-5-aminopyridine is employed for the development of new materials with specific properties, such as improved stability or reactivity.
Used in Biological Research:
2-Fluoro-3-methyl-5-aminopyridine is used as a drug targeting the central nervous system, offering potential therapeutic benefits for neurological disorders. Additionally, it serves as a valuable tool for studying neuronal functions and understanding the underlying mechanisms of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 186593-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,5,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 186593-48:
(8*1)+(7*8)+(6*6)+(5*5)+(4*9)+(3*3)+(2*4)+(1*8)=186
186 % 10 = 6
So 186593-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H7FN2/c1-4-2-5(8)3-9-6(4)7/h2-3H,8H2,1H3
186593-48-6Relevant academic research and scientific papers
3-Pyridyl enantiomers and their use as analgesics
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, (2008/06/13)
The present invention relates to a method of controlling pain in mammals, including humans, comprising administering to a mammal or patient in need of treatment thereof selected compounds of formula I: STR1 or a pharmaceutically acceptable salt thereof. The invention further relates to selected (R) and (S) compounds of formula I above which are useful as analgesics as well as neuronal cell death preventors and anti-inflammatories.
