444120-93-8 Usage
Description
2-Fluoro-5-(4-methoxyphenyl)pyridine is a pyridine derivative with the molecular formula C12H10FNO. It features a fluorine atom at the 2-position and a 4-methoxyphenyl group at the 5-position, which endows it with unique properties. This chemical compound is a valuable intermediate in organic synthesis and pharmaceutical research due to its specific chemical structure and functional groups.
Uses
Used in Pharmaceutical Research:
2-Fluoro-5-(4-methoxyphenyl)pyridine is used as a building block for the development of therapeutic drugs and agrochemicals. Its unique properties and specific chemical structure make it suitable for creating biologically active compounds, contributing to the advancement of medicinal chemistry and the discovery of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Fluoro-5-(4-methoxyphenyl)pyridine serves as a key intermediate. Its functional groups facilitate the synthesis of a variety of complex organic molecules, making it an essential component in the creation of diverse chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 444120-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,1,2 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 444120-93:
(8*4)+(7*4)+(6*4)+(5*1)+(4*2)+(3*0)+(2*9)+(1*3)=118
118 % 10 = 8
So 444120-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H10FNO/c1-15-11-5-2-9(3-6-11)10-4-7-12(13)14-8-10/h2-8H,1H3
444120-93-8Relevant articles and documents
A general Suzuki cross-coupling reaction of heteroaromatics catalyzed by nanopalladium on amino-functionalized siliceous mesocellular foam
Bratt, Emma,Verho, Oscar,Johansson, Magnus J,Baeckvall, Jan-Erling
, p. 3946 - 3954 (2014/05/20)
Suzuki-Miyaura cross-coupling reactions of heteroaromatics catalyzed by palladium supported in the cavities of amino-functionalized siliceous mesocellular foam are presented. The nanopalladium catalyst effectively couples not only heteroaryl halides with
Evaluation of 4′-substituted bicyclic pyridones as non-steroidal inhibitors of steroid 5α-reductase
McCarthy, Anna R.,Hartmann, Rolf W.,Abell, Andrew D.
, p. 3603 - 3607 (2008/02/08)
4′-Substituted bicyclic pyridones were prepared and evaluated as non-steroidal inhibitors of type 1 and 2 steroid 5α-reductase (SR). A range of 4′-substituents were incorporated into the bicyclic scaffold to investigate SAR within and across different cla
