14403-31-7 Usage
Uses
Used in Organic Synthesis:
Benzene, 1-bromo-2-(methylseleno)is used as a key intermediate in organic synthesis for the production of various organic compounds. Its unique structure allows for further functionalization and modification, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Benzene, 1-bromo-2-(methylseleno)is employed as a starting material or a precursor in the development of new drugs. Its potential bioactivity and unique chemical properties make it a promising candidate for the discovery of novel therapeutic agents.
Used in Medicinal Chemistry:
Benzene, 1-bromo-2-(methylseleno)exhibits potential bioactivity, which makes it a valuable compound in medicinal chemistry. Researchers can explore its interactions with biological targets and evaluate its efficacy in treating various diseases or conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 14403-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,0 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14403-31:
(7*1)+(6*4)+(5*4)+(4*0)+(3*3)+(2*3)+(1*1)=67
67 % 10 = 7
So 14403-31-7 is a valid CAS Registry Number.
14403-31-7Relevant academic research and scientific papers
Solvent-controlled halo-selective selenylation of aryl halides catalyzed by Cu(II) supported on Al2O3. A general protocol for the synthesis of unsymmetrical organo mono- and bis-selenides
Chatterjee, Tanmay,Ranu, Brindaban C.
, p. 7145 - 7153 (2013/08/23)
Alumina-supported Cu(II) efficiently catalyzes selenylation of aryl iodides and aryl bromides by diaryl, dialkyl, and diheteroaryl diselenides in water and PEG-600, respectively, leading to a general route toward synthesis of unsymmetrical diaryl, aryl-alkyl, aryl-heteroaryl, and diheteroaryl selenides. A sequential reaction of bromoiodobenzene with one diaryl/diheteroaryl/dialkyl diselenide in water and another diaryl/diheteroaryl/dialkyl diselenide in PEG-600 in the second step produces unsymmetrical diaryl, diheteroaryl, or aryl-alkyl bis-selanyl benzene. A library of functionalized organo mono- and bis-selenides, including a potent biologically active molecule and a couple of analogues of bioactive selenides, were obtained in high yields by this protocol. The reactions are chemoselective and high yielding. The Cu-Al2O 3 catalyst is recycled for seven runs without any appreciable loss of activity.
