131674-41-4 Usage
Uses
Used in Organic Synthesis:
3-(2-Methoxypyridin-3-yl)acrylic acid is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure and reactivity contribute to the formation of a variety of chemical entities, enhancing the diversity of synthesized compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-(2-Methoxypyridin-3-yl)acrylic acid is utilized as a key component in the development of new drugs. Its distinctive chemical properties allow for the exploration of its potential therapeutic effects and incorporation into novel medicinal compounds.
Used in Material Development:
3-(2-Methoxypyridin-3-yl)acrylic acid may also be employed in the development of new materials, leveraging its structural and reactive attributes to engineer innovative substances with specific properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 131674-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,6,7 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 131674-41:
(8*1)+(7*3)+(6*1)+(5*6)+(4*7)+(3*4)+(2*4)+(1*1)=114
114 % 10 = 4
So 131674-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO3/c1-13-9-7(3-2-6-10-9)4-5-8(11)12/h2-6H,1H3,(H,11,12)
131674-41-4Relevant academic research and scientific papers
Small molecule inhibitors of anthrax lethal factor toxin
Williams, John D.,Khan, Atiyya R.,Cardinale, Steven C.,Butler, Michelle M.,Bowlin, Terry L.,Peet, Norton P.
supporting information, p. 419 - 434 (2014/01/17)
This manuscript describes the preparation of new small molecule inhibitors of Bacillus anthracis lethal factor. Our starting point was the symmetrical, bis-quinolinyl compound 1 (NSC 12155). Optimization of one half of this molecule led to new LF inhibitors that were desymmetrized to afford more drug-like compounds.
Improved Synthesis of 2,3-Disubstituted Pyridines by Metallation of 2-Chloropyridine: a Convenient Route to Fused Polyheterocycles
Trecourt, Francois,Marsais, Francis,Guengoer, Timur,Queguiner, Guy
, p. 2409 - 2415 (2007/10/02)
Chemoselective directed metallation of 2-chloropyridine allows the synthesis of 2-substituted 3-carbonylated pyridines, advantage being taken of the metallation ortho-directing effect of the halogen, as well as its reactivity towards nucleophiles.Thus (2-chloro-, 2-methoxy-, and 2-amino-3-pyridyl)-ethanones and -arylmethanones as well as carbaldehydes have been prepared.Some of these ortho-disubstituted intermediates have been readily cyclized to fused polyheterocycles such as naphthiridines and aza-analoges of coumarins, xanthones, and acridones.
