50630-23-4 Usage
Description
[(2-bromoethyl)selanyl]benzene is a chemical compound characterized by a benzene ring with a selenyl group and a bromoethyl group attached. It is identified by the chemical formula C8H9BrSe and is recognized for its potential applications in organic synthesis, chemical reactions, medicinal chemistry, and pharmaceuticals due to its ability to engage in various biological processes. Furthermore, it may serve as a precursor in the synthesis of other organoselenium and organobromine compounds. Handling this chemical agent requires adherence to proper safety protocols.
Uses
Used in Organic Synthesis:
[(2-bromoethyl)selanyl]benzene is used as a building block in the synthesis of complex organic molecules, contributing to the structural diversity and functional properties of the resulting compounds.
Used in Chemical Reactions:
As a reagent, [(2-bromoethyl)selanyl]benzene is employed in various chemical reactions to facilitate specific transformations, enhancing the efficiency and selectivity of the processes.
Used in Medicinal Chemistry:
[(2-bromoethyl)selanyl]benzene is utilized as a compound of interest in medicinal chemistry, where its unique structural features and reactivity may contribute to the development of novel therapeutic agents.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(2-bromoethyl)selanyl]benzene is used as a precursor for the synthesis of organoselenium and organobromine compounds, which may possess valuable pharmacological properties and applications in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 50630-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50630-23:
(7*5)+(6*0)+(5*6)+(4*3)+(3*0)+(2*2)+(1*3)=84
84 % 10 = 4
So 50630-23-4 is a valid CAS Registry Number.
50630-23-4Relevant articles and documents
Remarkable alkene-to-alkene and alkene-to-alkyne transfer reactions of selenium dibromide and phsebr. Stereoselective addition of selenium dihalides to cycloalkenes
Potapov, Vladimir A.,Musalov, Maxim V.,Kurkutov, Evgeny O.,Yakimov, Vladimir A.,Khabibulina, Alfiya G.,Musalova, Maria V.,Amosova, Svetlana V.,Borodina, Tatyana N.,Albanov, Alexander I.
, (2020/01/13)
The original goal of this research was to study stereochemistry of selenium dihalides addition to cycloalkenes and properties of obtained products. Remarkable alkene-to-alkene and alkene-to-alkyne transfer reactions of selenium dibromide and PhSeBr were discovered during this research. The adducts of selenium dibromide with alkenes or cycloalkenes easily exchange SeBr2 with other unsaturated compounds, including acetylenes, at room temperature, in acetonitrile. Similar alkene-to-alkene and alkene-to-alkyne transfer reactions of the PhSeBr adducts with alkenes or cycloalkenes take place. The supposed reaction pathway includes the selenium group transfer from seleniranium species to alkenes or alkynes. It was found that the efficient SeBr2 and PhSeBr transfer reagents are Se(CH2CH2Br)2 and PhSeCH2CH2Br, which liberate ethylene, leading to a shift in equilibrium. The regioselective and stereoselective synthesis of bis(E-2-bromovinyl) selenides and unsymmetrical E-2-bromovinyl selenides was developed based on the SeBr2 and PhSeBr transfer reactions which proceeded with higher selectivity compared to analogous addition reactions of SeBr2 and PhSeBr to alkynes under the same conditions.
