351456-48-9 Usage
Uses
Used in Chemical Research:
3,5-Diiodo (1H) indazole is used as a research compound for exploring its chemical properties and potential applications in the synthesis of more complex compounds. Its unique structure, which includes the indazole moiety and iodine atoms, may offer insights into the development of new chemical reactions and pathways.
Used in Pharmaceutical Development:
While not explicitly mentioned in the provided materials, the indazole class of compounds is known for its potential in pharmaceutical applications. 3,5-Diiodo (1H) indazole could be used as a starting material or intermediate in the development of new drugs, particularly in the areas of oncology, where indazole-based compounds have shown promise as anticancer agents. Its halogenated nature may also contribute to its potential use in medicinal chemistry, where halogenated compounds are often employed for their unique reactivity and properties.
Used in Material Science:
The presence of iodine atoms in 3,5-Diiodo (1H) indazole may also make it a candidate for use in material science, particularly in the development of new materials with specific properties. For example, its halogenated nature could be exploited in the synthesis of materials with unique electronic, optical, or magnetic properties, or in the creation of new catalysts for chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 351456-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,4,5 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 351456-48:
(8*3)+(7*5)+(6*1)+(5*4)+(4*5)+(3*6)+(2*4)+(1*8)=139
139 % 10 = 9
So 351456-48-9 is a valid CAS Registry Number.
351456-48-9Relevant academic research and scientific papers
Synthesis of new dehydro 2-azatryptophans and derivatives via Heck cross-coupling reactions of 3-iodoindazoles with methyl 2-(acetylamino)acrylate
Crestey, Francois,Collot, Valerie,Stiebing, Silvia,Rault, Sylvain
, p. 3506 - 3514 (2008/02/10)
This paper describes the Heck cross-coupling reaction of 3-iodoindazoles with methyl 2-(acetylamino)acrylate as a general route to new dehydro 2-azatryptophans and protected amino acid derivatives after catalytic hydrogenation. Georg Thieme Verlag Stuttgart.
