817172-42-2 Usage
Description
2-(3-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE is a chemical compound with the molecular formula C14H9N3O3. It is a derivative of imidazo[1,2-a]pyridine and contains a nitrophenyl group and a carboxaldehyde functional group. 2-(3-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE is commonly used in organic synthesis and medicinal chemistry research due to its unique structure and potential biological activities. Its properties and reactivity make it a valuable building block for the synthesis of various heterocyclic compounds and potential drug candidates. The nitro group in the 3-position of the phenyl ring makes it a potential candidate for the development of new drugs with anti-inflammatory, antimicrobial, or antitumor activities.
Uses
Used in Organic Synthesis:
2-(3-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE is used as a building block for the synthesis of various heterocyclic compounds. Its unique structure and reactivity make it a valuable component in the creation of complex organic molecules.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-(3-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE is used as a starting material for the development of potential drug candidates. Its properties and potential biological activities make it a promising candidate for further research and development.
Used in Pharmaceutical Development:
2-(3-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE is used as a potential candidate for the development of new drugs with anti-inflammatory, antimicrobial, or antitumor activities. The nitro group in the 3-position of the phenyl ring contributes to its potential therapeutic applications.
Used in Chemical Research:
In the realm of chemical research, 2-(3-NITRO-PHENYL)-IMIDAZO[1,2-A]PYRIDINE-3-CARBOXALDEHYDE is used to study its properties and reactivity. This helps researchers to better understand its potential uses and to develop new methods for its synthesis and application.
Check Digit Verification of cas no
The CAS Registry Mumber 817172-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,1,7 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 817172-42:
(8*8)+(7*1)+(6*7)+(5*1)+(4*7)+(3*2)+(2*4)+(1*2)=162
162 % 10 = 2
So 817172-42-2 is a valid CAS Registry Number.
817172-42-2Relevant articles and documents
Exploration of the CuAAC reaction for the synthesis of novel 3-(triazol-1-yl)methyl-imidazo[1,2-a]pyridines
Khedar, Poonam,Pericherla, Kasiviswanadharaju,Kumar, Anil
, p. 2609 - 2614,6 (2012/12/12)
The archetypical CuAAC click chemistry is explored to assemble diverse 3-(triazol-1-yl)methyl-imidazo[1,2-a]pyridines. The approach is simple, general, and environmentally benign to generate a library of novel triazolo-imidazo[1,2- a]pyridine derivatives in good yield (30-90%).
