• 1. An artificial CO-releasing metalloprotein built by histidine-selective metallation?
  Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
• 2. Acentric and chiral heterometallic inorganic–organic hybrid frameworks mediated by alkali or alkaline earth ions: synthesis and NLO properties
  Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
• 3. An air-stable organometallic polymer containing titanafluorene moieties obtained by the Sonogashira–Hagihara cross-coupling polycondensation?
  Alvin Tanudjaja,Shinsuke Inagi,Fusao Kitamura,Toshikazu Takata,Ikuyoshi Tomita Dalton Trans., 2021,50, 3037-3043
• 4. An amphoteric reactivity of a mixed-valent bis(μ-oxo)dimanganese(iii,iv) complex acting as an electrophile and a nucleophile?
  Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
• 5. An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes?
  Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873

• Solvents and Organic Chemicals Organic Compounds Organic 1,3-dipolar compounds Allyl-type 1,3-dipolar organic compounds C-nitro compounds
• Solvents and Organic Chemicals Organic Compounds Organic 1,3-dipolar compounds Allyl-type 1,3-dipolar organic compounds Organic nitro compounds C-nitro compounds

2,5-Dibromo-4-nitropyridin-1-ium-1-olate: A Comprehensive Overview

The compound with CAS No. 221241-25-4, commonly referred to as 2,5-Dibromo-4-nitropyridin-1-ium-1-olate, is a highly specialized organic compound that has garnered significant attention in the fields of organic synthesis, materials science, and pharmacology. This compound is characterized by its unique structure, which includes a pyridinium ring substituted with bromine atoms at positions 2 and 5, and a nitro group at position 4. The presence of these substituents imparts distinctive electronic and steric properties to the molecule, making it a valuable tool in various research and industrial applications.

Recent advancements in synthetic chemistry have enabled the precise synthesis of 2,5-Dibromo-4-nitropyridin-1-ium-1-olate, leveraging innovative methodologies such as microwave-assisted synthesis and catalytic processes. These techniques not only enhance the efficiency of the synthesis but also contribute to the sustainability of chemical production by minimizing waste and energy consumption. The compound's ability to act as both an electrophilic and nucleophilic species makes it a versatile building block in organic synthesis.

In the realm of materials science, 2,5-Dibromo-4-nitropyridin-1-ium-1-olate has been explored for its potential in the development of advanced materials such as conductive polymers and coordination networks. Its ability to form stable coordination complexes with transition metals has opened new avenues for creating materials with tailored electronic properties. For instance, researchers have demonstrated that this compound can serve as a ligand in metalloporphyrin systems, which exhibit promising applications in catalysis and sensing technologies.

The pharmacological potential of 2,5-Dibromo-4-nitropyridin-1-ium-1-olate has also been a focal point of recent studies. Investigations into its biological activity have revealed that it exhibits selective cytotoxicity against certain cancer cell lines, suggesting its potential as a lead compound for anticancer drug development. Furthermore, its ability to modulate cellular signaling pathways makes it a candidate for exploring novel therapeutic strategies.

From an environmental standpoint, the stability and biodegradability of 2,5-Dibromo-4-nitropyridin-1ium-1-olate have been rigorously evaluated to ensure its safe use in industrial settings. Regulatory frameworks governing chemical safety have played a pivotal role in shaping its application across various sectors.

In conclusion, 2,5-Dibromo-4-nitropyridin-1-ium-1-olate stands as a testament to the ingenuity of modern chemistry. Its multifaceted applications across diverse fields underscore its significance as a key compound in contemporary scientific research. As ongoing studies continue to unravel its potential, this compound is poised to play an even more prominent role in shaping future innovations.

• 1678-49-5(3-bromo-4-nitropyridine 1-oxide)
• 118619-26-4(3-bromo-4-nitro-1-oxidopyridin-1-ium,perchloric acid)
• 98027-81-7(2,6-Dibromo-4-nitropyridine oxide)
• 52092-43-0(2-bromo-4-nitro-1-oxido-pyridin-1-ium)
• 1804419-87-1(2,3-Dibromo-4-nitropyridine)
• 221241-31-2(2,5-Dibromo-4-nitropyridine)
• 62516-09-0(Pyridine,3,5-dibromo-4-nitro-, 1-oxide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)