437709-98-3 Usage
Uses
Used in Organic Synthesis:
2,6-Diiodo-3-methoxypyridine is used as a building block for the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of new molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,6-Diiodo-3-methoxypyridine is utilized as a reagent in the preparation of pharmaceutical compounds. Its presence in these compounds can contribute to their biological activity and therapeutic potential.
Used as a Precursor in Synthesis:
2,6-Diiodo-3-methoxypyridine also serves as a potential precursor in the synthesis of biologically active molecules. Its structural features make it a promising candidate for the development of new drugs and pharmaceutical agents.
Used in the Synthesis of Novel Materials:
Furthermore, 2,6-Diiodo-3-methoxypyridine has shown potential as a reagent for the synthesis of novel materials with interesting properties. Its incorporation into these materials can lead to unique characteristics and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 437709-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,7,7,0 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 437709-98:
(8*4)+(7*3)+(6*7)+(5*7)+(4*0)+(3*9)+(2*9)+(1*8)=183
183 % 10 = 3
So 437709-98-3 is a valid CAS Registry Number.
437709-98-3Relevant academic research and scientific papers
First synthesis of caerulomycin B. A new synthesis of caerulomycin C.
Mongin, Florence,Trecourt, Francois,Gervais, Bruno,Mongin, Olivier,Queguiner, Guy
, p. 3272 - 3276 (2007/10/03)
Caerulomycins produced by Streptomyces caeruleus are bipyridinic molecules endowed with antibiotic properties. The first synthesis of caerulomycin B (1) as well as a new synthesis of caerulomycin C (2) are reported. Starting from 3-hydroxypyridine, the same methodology was used to prepare both compounds 1 and 2. Efficiently controlled reactions such as metalation to allow the synthesis of 2,6-diiodo-3,4-dialkoxypyridines, which are key intermediates, and further halogen-lithium exchange and cross-coupling to reach the targets molecules 1 and 2 have been developed.
