750638-97-2 Usage
Uses
Used in Organic Synthesis:
2,4-Diiodo-3-hydroxypyridine is utilized as a building block in organic synthesis for the production of pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a variety of complex organic molecules, making it a valuable component in the development of new drugs and chemical products.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,4-Diiodo-3-hydroxypyridine is used as a precursor for the synthesis of compounds with potential therapeutic applications. Its anti-cancer and anti-inflammatory properties are of particular interest, as they may contribute to the development of new treatments for various diseases.
Used in Imaging Agents for PET Scans:
2,4-Diiodo-3-hydroxypyridine has been investigated for its potential use in the development of imaging agents for positron emission tomography (PET) scans. Its unique properties may allow for the creation of radiolabeled compounds that can be used to visualize biological processes in vivo, providing valuable diagnostic information for medical professionals.
Check Digit Verification of cas no
The CAS Registry Mumber 750638-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,0,6,3 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 750638-97:
(8*7)+(7*5)+(6*0)+(5*6)+(4*3)+(3*8)+(2*9)+(1*7)=182
182 % 10 = 2
So 750638-97-2 is a valid CAS Registry Number.
750638-97-2Relevant academic research and scientific papers
Preparation of functionalized 3,4-pyridynes via 2-magnesiated diaryl sulfonates
Lin, Wenwei,Chen, Ling,Knochel, Paul
, p. 2787 - 2797 (2007/10/03)
The preparation of functionalized 3,4-pyridynes of type 1 as highly reactive intermediates has been achieved by the controlled elimination of readily generated 2-magnesiated diaryl sulfonates of type 2 obtained by a low temperature I/Mg- or Br/Mg-exchange starting from the corresponding halides of type 3. After trapping with furan, moderate to good yields of the desired functionalized cycloadducts of type 4 are obtained. The addition of a magnesium arylthiolate or magnesium phenylselenide to 3,4-pyridyne followed by quenching with an electrophile is also described.
