Cas no 685862-28-6 (1,2-Bis((5-bromopyridin-2-yl)oxy)ethane)

1,2-Bis((5-bromopyridin-2-yl)oxy)ethane is a brominated pyridine derivative with a symmetrical ethane-linked structure, offering utility as a versatile intermediate in organic synthesis. Its key advantages include the presence of reactive bromine substituents, which facilitate further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig couplings. The ethoxy linker enhances molecular flexibility, making it suitable for constructing complex architectures in pharmaceuticals, agrochemicals, and materials science. The compound's high purity and stability under standard conditions ensure reliable performance in synthetic applications. Its well-defined structure also allows for precise modification, enabling tailored design of target molecules in research and industrial settings.
1,2-Bis((5-bromopyridin-2-yl)oxy)ethane structure
685862-28-6 structure
Product Name:1,2-Bis((5-bromopyridin-2-yl)oxy)ethane
CAS No:685862-28-6
MF:C12H10Br2N2O2
MW:374.028001308441
MDL:MFCD19704311
CID:1034522
PubChem ID:71302011
Update Time:2025-10-12

1,2-Bis((5-bromopyridin-2-yl)oxy)ethane Chemical and Physical Properties

Names and Identifiers

    • 1,2-Bis((5-bromopyridin-2-yl)oxy)ethane
    • 1,2-BIS(5-BROMOPYRIDIN-2-YLOXY)ETHANE
    • 5-bromo-2-[2-(5-bromopyridin-2-yl)oxyethoxy]pyridine
    • 2,2'-[1,2-ethanediylbis(oxy)]bis[5-bromopyridine]
    • AK131375
    • KB-10058
    • RL04620
    • AKOS016014851
    • C12H10Br2N2O2
    • 5-BROMO-2-{2-[(5-BROMOPYRIDIN-2-YL)OXY]ETHOXY}PYRIDINE
    • 2,2'-[Ethane-1,2-diylbis(oxy)]bis(5-bromopyridine)
    • DTXSID40744496
    • 685862-28-6
    • J-503799
    • DB-311376
    • MDL: MFCD19704311
    • Inchi: 1S/C12H10Br2N2O2/c13-9-1-3-11(15-7-9)17-5-6-18-12-4-2-10(14)8-16-12/h1-4,7-8H,5-6H2
    • InChI Key: GQRBSNHPIYDQPX-UHFFFAOYSA-N
    • SMILES: BrC1=CN=C(C=C1)OCCOC1C=CC(=CN=1)Br

Computed Properties

  • Exact Mass: 373.90885g/mol
  • Monoisotopic Mass: 371.91090g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 5
  • Complexity: 222
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.5
  • Topological Polar Surface Area: 44.2?2

1,2-Bis((5-bromopyridin-2-yl)oxy)ethane Pricemore >>

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Additional information on 1,2-Bis((5-bromopyridin-2-yl)oxy)ethane

1,2-Bis((5-bromopyridin-2-yl)oxy)ethane: A Comprehensive Overview

1,2-Bis((5-bromopyridin-2-yl)oxy)ethane, also known by its CAS number 685862-28-6, is a chemical compound that has garnered significant attention in the fields of organic chemistry and materials science. This compound is characterized by its unique structure, which combines a pyridine ring with bromine substituents and ethylene glycol linkages. The molecule's structure makes it a versatile building block for various applications, particularly in the synthesis of advanced materials and pharmaceuticals.

The compound's name, 1,2-Bis((5-bromopyridin-2-yl)oxy)ethane, reflects its structural composition. The pyridine ring is a six-membered aromatic ring with one nitrogen atom, and the bromine substituent at the 5-position adds electronic complexity. The ethylene glycol backbone connects two such pyridine units via oxygen atoms, forming a symmetrical structure. This symmetry is crucial for its chemical reactivity and potential applications.

Recent studies have highlighted the importance of compounds like 1,2-Bis((5-bromopyridin-2-yl)oxy)ethane in the development of coordination polymers and metal-organic frameworks (MOFs). These materials are highly sought after due to their potential in gas storage, catalysis, and sensing applications. The bromine substituents in the pyridine rings act as coordinating groups, enabling the formation of robust networks with metal ions.

In addition to its role in materials science, this compound has shown promise in medicinal chemistry. Its ability to act as a chelating agent makes it a candidate for designing drugs targeting metalloenzymes or metalloproteins. Recent research has explored its interactions with transition metals like copper and zinc, which are critical for various biological processes.

The synthesis of 1,2-Bis((5-bromopyridin-2-yl)oxy)ethane typically involves multi-step reactions, including nucleophilic substitution and coupling reactions. The choice of starting materials and reaction conditions plays a pivotal role in achieving high yields and purity. Researchers have optimized these conditions to minimize side reactions and improve scalability.

From an environmental standpoint, understanding the degradation pathways of 1,2-Bis((5-bromopyridin-2-yl)oxy)ethane is essential for assessing its ecological impact. Studies have shown that under certain conditions, such as UV light or microbial activity, the compound undergoes hydrolysis or oxidation, leading to the formation of less complex products. These findings are crucial for developing sustainable synthetic routes and waste management strategies.

In conclusion, 1,2-Bis((5-bromopyridin-2-yl)oxy)ethane (CAS No: 685862-28-6) is a multifaceted compound with applications spanning materials science and medicinal chemistry. Its unique structure and reactivity make it a valuable tool for researchers aiming to develop innovative materials and therapies. As ongoing studies continue to uncover new properties and applications, this compound is poised to play an increasingly important role in various scientific disciplines.

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