2,2'-Bipyridine, 4-bromo-


Chemical Name: 2,2'-Bipyridine, 4-bromo-
CAS Number: 14162-95-9
Product Number: AG001GP7(AGN-PC-0NHQQV)
Synonyms:
MDL No:
Molecular Formula: C10H7BrN2
Molecular Weight: 235.0800

Identification/Properties


Properties
BP:
325.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
235.084g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
233.979g/mol
Monoisotopic Mass:
233.979g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
163
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



4-Bromo-2,2'-bipyridine is a versatile chemical compound used extensively in chemical synthesis as a key building block for designing and creating various organic molecules. This compound serves as a valuable reagent in the preparation of complex coordination complexes and metal-organic frameworks due to its unique structural features and reactivity.One of the prominent applications of 4-Bromo-2,2'-bipyridine is in the field of coordination chemistry, where it acts as a ligand to form coordination complexes with various metal ions. These complexes find wide applications in catalysis, materials science, and medicinal chemistry. The presence of the bromine group in the compound allows for facile functionalization, enabling the incorporation of additional substituents or functional groups to tailor the properties of the resulting complexes.Additionally, 4-Bromo-2,2'-bipyridine is often employed in the synthesis of organic molecules with specialized properties, such as fluorescent dyes, pharmaceutical intermediates, and molecular sensors. Its rigid bipyridine backbone imparts structural rigidity and precise spatial orientation to the molecules, making it particularly useful in supramolecular chemistry and the construction of molecular assemblies with predictable architectures.Furthermore, the halogen substituent in 4-Bromo-2,2'-bipyridine can participate in various cross-coupling reactions, such as Suzuki-Miyaura or Heck coupling, facilitating the synthesis of more complex molecular structures. This compound's versatility and reactivity make it a valuable tool for organic chemists and researchers working in the fields of chemical synthesis and materials science.