339155-02-1 Usage
Uses
Used in Organic Synthesis:
[2,2'-Bipyridin]-4-yl-phenyl-methanone is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different properties and applications.
Used in Coordination Chemistry:
As a ligand, [2,2'-Bipyridin]-4-yl-phenyl-methanone is used in coordination chemistry to form complexes with metal ions. These complexes have potential applications in areas such as catalysis, sensing, and materials science.
Used in Medicinal Chemistry:
[2,2'-Bipyridin]-4-yl-phenyl-methanone is used as a building block for the development of new drugs and pharmaceuticals. Its potential biological and pharmacological properties make it a promising candidate for the treatment of various diseases and conditions.
Used in the Synthesis of New Materials:
[2,2'-Bipyridin]-4-yl-phenyl-methanone has potential applications in the development of new materials and compounds with unique properties, such as improved stability, reactivity, or selectivity. These materials could be used in various industries, including electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 339155-02-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,1,5 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 339155-02:
(8*3)+(7*3)+(6*9)+(5*1)+(4*5)+(3*5)+(2*0)+(1*2)=141
141 % 10 = 1
So 339155-02-1 is a valid CAS Registry Number.
339155-02-1Relevant academic research and scientific papers
From Pyridine- N-oxides to 2-Functionalized Pyridines through Pyridyl Phosphonium Salts: An Umpolung Strategy
Bugaenko, Dmitry I.,Yurovskaya, Marina A.,Karchava, Alexander V.
supporting information, p. 6099 - 6104 (2021/08/03)
The reactions of pyridine-N-oxides with Ph3P under the developed conditions provide an unprecedented route to (pyridine-2-yl)phosphonium salts. Upon activation with DABCO, these salts readily serve as functionalized 2-pyridyl nucleophile equivalents. This umpolung strategy allows for the selective C2 functionalization of the pyridine ring with electrophiles, avoiding the generation and use of unstable organometallic reagents. The protocol operates at ambient temperature and tolerates sensitive functional groups, enabling the synthesis of otherwise challenging compounds.
2,2′-Bipyridines carrying a diazo moiety and their complexes with bis(hexafluoroacetylacetonato)copper: Synthesis, structures, electronic and magnetic properties of their photoproducts in frozen solutions
Morikawa,Imamura,Tsurukami,Itoh,Kumada,Karasawa,Koga,Iwamura
, p. 493 - 502 (2007/10/03)
4-(α-Diazobenzyl)-2,2′-bipyridine 2, diazodi{4-(2,2′-bipyridyl)}methane 3, and 1,3-benzenediyl{4-(4′-methyl-2.2°prime;-bipyridyl)diazomethane} 4 were prepared as new types of spin sources/magnetic couplers. The molecular structures of bipyridine ligands,
