• 1. Excitable dynamics in the bromate–sulfite–ferrocyanide reaction
  J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
• 2. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
  Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
• 3. EWOD-driven droplet microfluidic device integrated with optoelectronic tweezers as an automated platform for cellular isolation and analysis?
  Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
• 4. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
• 5. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?
  Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Imidazopyridines Imidazopyridines
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Imidazopyridines
• Solvents and Organic Chemicals Organic Compounds Alcohol/Ether

The Chemistry and Applications of {imidazo[1,2-a]pyridin-3-yl}methanol (CAS No. 30489-43-1)

{imidazo[1,2-a]pyridin-3-yl}methanol, also known by its CAS number 30489-43-1, is a heterocyclic compound with significant potential in various chemical and pharmaceutical applications. This compound belongs to the class of imidazopyridines, which are known for their unique electronic properties and structural versatility. The molecule consists of an imidazo[1,2-a]pyridine ring system attached to a methanol group, making it a valuable intermediate in organic synthesis.

The imidazo[1,2-a]pyridine core of this compound is a fused bicyclic structure comprising an imidazole ring fused to a pyridine ring. This arrangement imparts the molecule with aromaticity and conjugation, which are key factors in its reactivity and stability. The methanol group (-CH?OH) attached at the 3-position of the imidazo[1,2-a]pyridine ring introduces hydrophilic properties, enhancing its solubility in polar solvents. This makes {imidazo[1,2-a]pyridin-3-yl}methanol an ideal candidate for use in aqueous environments or as a precursor for more complex molecules.

Recent studies have highlighted the importance of {imidazo[1,2-a]pyridin-3-yl}methanol in drug discovery and development. Its structural flexibility allows for the incorporation of various functional groups, enabling the creation of bioactive compounds with potential therapeutic applications. For instance, researchers have explored its role as a building block for designing kinase inhibitors and other enzyme-targeting agents. The ability to modify the methanol group further expands its utility in medicinal chemistry.

In addition to its pharmaceutical applications, {imidazo[1,2-a]pyridin-3-yl}methanol has shown promise in materials science. Its aromaticity and conjugation make it a suitable candidate for use in organic electronics and optoelectronic devices. Recent advancements in this field have demonstrated that derivatives of this compound can exhibit desirable electronic properties, such as high electron mobility and photoluminescence efficiency. These characteristics position it as a potential material for use in light-emitting diodes (LEDs) and solar cells.

The synthesis of {imidazo[1,2-a]pyridin-3-yl}methanol typically involves multi-step organic reactions. One common approach involves the cyclization of appropriate precursors under acidic or basic conditions to form the imidazo[1,2-a]pyridine ring system. Subsequent functionalization steps allow for the introduction of the methanol group or other substituents. Recent research has focused on optimizing these synthetic routes to improve yield and selectivity while minimizing environmental impact.

From an environmental perspective, {imidazo[1,2-a]pyridin-3-yl}methanol has been studied for its biodegradability and toxicity profile. Initial findings suggest that it is not inherently hazardous under normal handling conditions; however, further studies are required to fully understand its environmental fate and potential risks.

In conclusion, {imidazo[1,2-a]pyridin-3-yl}methanol (CAS No. 30489-43-1) is a versatile compound with diverse applications across multiple disciplines. Its unique chemical structure and functional properties make it an invaluable tool in organic synthesis, drug discovery, and materials science. As research continues to uncover new possibilities for this compound, its role in advancing scientific innovation is expected to grow significantly.

• 167884-17-5({imidazo[1,2-a]pyridin-5-yl}methanol)
• 926223-25-8((6-Methylimidazo1,2-apyridin-2-yl)methanol)
• 1216294-32-4((7-Methylimidazo1,2-apyridin-2-yl)methanol)
• 872362-98-6((8-Methylimidazo1,2-apyridin-2-yl)methanol)
• 30489-44-2({2-methylimidazo1,2-apyridin-3-yl}methanol)
• 30489-62-4(Imidazo1,2-apyridin-3-ylmethanol hydrochloride)
• 668275-46-5((3-methylimidazo1,2-apyridin-2-yl)methanol)
• 82090-52-6({imidazo[1,2-a]pyridin-2-yl}methanol)
• 217435-75-1((2,7-dimethylH-imidazo[1,2-a]pyridin-3-yl)methanol)
• 873943-42-1((2,8-DIMETHYL-IMIDAZO[1,2-A]PYRIDIN-3-YL)-METHANOL)