• 1. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
• 2. Essential effect of the electrolyte on the mechanical and chemical degradation of LiNi0.8Co0.15Al0.05O2 cathodes upon long-term cycling??
  Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
• 3. Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis?
  Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
• 4. Excitable dynamics in the bromate–sulfite–ferrocyanide reaction
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• 5. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
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Pyridine, 3-bromo-5-methoxy-2-nitro-

The compound Pyridine, 3-bromo-5-methoxy-2-nitro- (CAS No. 1705547-96-1) is a highly specialized organic chemical with a unique molecular structure that makes it suitable for various applications in the fields of pharmaceuticals, agrochemicals, and materials science. This compound is characterized by its pyridine ring, which serves as the core structure, with substituents at positions 2, 3, and 5. The substituents include a nitro group (-NO?) at position 2, a bromine atom (Br) at position 3, and a methoxy group (-OCH?) at position 5. These functional groups impart specific chemical properties to the molecule, making it versatile for different synthetic pathways and applications.

Recent studies have highlighted the potential of Pyridine, 3-bromo-5-methoxy-2-nitro-, in the development of novel drug delivery systems. The nitro group at position 2 is known to enhance the compound's reactivity in certain reactions, while the methoxy group at position 5 contributes to its solubility in organic solvents. This combination of properties makes it an ideal candidate for use in the synthesis of bioactive molecules. For instance, researchers have explored its role in the creation of anti-inflammatory agents and anticancer drugs, where the bromine atom can act as a leaving group in substitution reactions.

In addition to its pharmaceutical applications, Pyridine, 3-bromo-5-methoxy-2-nitro-, has shown promise in the field of agrochemistry. The compound's ability to undergo various nucleophilic substitutions and oxidations has led to its use in the development of pesticides and herbicides. Recent advancements in green chemistry have also focused on optimizing the synthesis pathways of this compound to minimize environmental impact. For example, researchers have developed catalytic methods that reduce the use of hazardous reagents while maintaining high yields.

The physical properties of Pyridine, 3-bromo-5-methoxy-2-nitro-, such as its melting point and boiling point, are critical factors in determining its suitability for different industrial processes. The compound exhibits a melting point of approximately 120°C and a boiling point around 280°C under standard conditions. These properties make it stable under moderate thermal conditions, which is advantageous for large-scale manufacturing processes.

Furthermore, the compound's spectroscopic data has been extensively studied using techniques such as UV-Vis spectroscopy and NMR spectroscopy. These studies have provided insights into the electronic transitions and molecular interactions within the molecule. For instance, the presence of the nitro group at position 2 leads to strong absorption bands in the UV region, which can be exploited for sensing applications.

In conclusion, Pyridine, 3-bromo-5-methoxy-2-nitro-, with its unique combination of functional groups and favorable physical properties, continues to be a valuable compound in various scientific disciplines. Its role in drug development, agrochemistry, and materials science underscores its importance as a versatile building block for advanced chemical compounds.

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