1094-77-5 Usage
Uses
Used in Pharmaceutical Research:
2-(2-benzylpyridin-1(2H)-yl)-1-phenylethanone is utilized as a building block in the synthesis of various biologically active molecules. Its role in this capacity is crucial for the development of new pharmaceutical agents.
Used in Neurological Disorders Treatment:
2-(2-benzylpyridin-1(2H)-yl)-1-phenylethanone is being studied for its potential pharmacological properties, particularly in the context of treating neurological disorders. Its specific mechanisms and effects are under investigation to determine its therapeutic potential in this area.
Used as an Anti-Inflammatory Agent:
2-(2-benzylpyridin-1(2H)-yl)-1-phenylethanone is also being explored for its potential as an anti-inflammatory agent. 2-(2-benzylpyridin-1(2H)-yl)-1-phenylethanone's ability to modulate inflammation could have significant implications for the treatment of various inflammatory conditions.
Used in Chemical and Medicinal Chemistry Research:
Due to its unique structure and properties, 2-(2-benzylpyridin-1(2H)-yl)-1-phenylethanone serves as a valuable tool in chemical and medicinal chemistry research. It aids in the understanding of molecular interactions and the development of novel therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 1094-77-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1094-77:
(6*1)+(5*0)+(4*9)+(3*4)+(2*7)+(1*7)=75
75 % 10 = 5
So 1094-77-5 is a valid CAS Registry Number.
1094-77-5Relevant academic research and scientific papers
Li, Ke,Li, Changkun
, p. 9456 - 9461 (2020)
The first highly regio- and enantioselective synthesis of 3-allylindolizines has been developed by the sequential Rh-catalyzed asymmetric allylation and Tschitschibabin reaction. Above the 20:1 branch/linear ratio, up to a 96% yield and 99% ee could be obtained with the help of tert-butyl-substituted chiral bisoxazolinephosphine ligand. In situ generated highly nucleophilic 2-alkylpyridinium ylides are utilized to undergo the asymmetric alkylation reaction before cyclization.
Method and composition for rejuvinating cells, tissues organs, hair and nails
-
, (2008/06/13)
In one embodiment, the present invention relates to compounds and compositions including pharmaceutical compositions containing the compounds and associated methods that uncouple sugar-mediated coupling of proteins, lipids, nucleic acids, and other biomat
2-Phosphaindolizines
Bansal, Raj K.,Karaghiosoff, Konstantin,Gupta, Neelima,Schmidpeter, Alfred,Spindler, Claudia
, p. 475 - 480 (2007/10/02)
Pyridinium bromides 3 prepared by alkylation of 2-methyl-, 2-ethyl-, and 2-benzylpyridines 1 with methyl bromides 2 bearing an electron-withdrawing group (COPh, CN, CO2Et, C6H4NO2) are condensed with PCl3 in the presence of Et3N to give 2-phosphaindolizin
