15733-05-8 Usage
Uses
Used in Pharmaceutical Industry:
Sulfone, 1,2-diphenylethyl methyl (8CI) is used as an intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, Sulfone, 1,2-diphenylethyl methyl (8CI) is utilized as an intermediate in the production of various agrochemicals. Its properties make it suitable for the synthesis of compounds with pesticidal, herbicidal, or other agricultural applications.
Used in Organic Synthesis:
Sulfone, 1,2-diphenylethyl methyl (8CI) is employed as a building block in organic synthesis. Its sulfonyl group and 1,2-diphenylethyl group provide opportunities for further chemical reactions, enabling the creation of a wide range of organic compounds with diverse applications.
Used in Material Science:
Sulfone, 1,2-diphenylethyl methyl (8CI) has been studied for its potential applications in material science. Its unique structure and properties make it a promising candidate for the development of new materials with specific characteristics, such as improved thermal stability, mechanical strength, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 15733-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,7,3 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15733-05:
(7*1)+(6*5)+(5*7)+(4*3)+(3*3)+(2*0)+(1*5)=98
98 % 10 = 8
So 15733-05-8 is a valid CAS Registry Number.
15733-05-8Relevant academic research and scientific papers
The leaving group dependence in the rates of solvolysis of 1,2-diphenylethyl system
Santhosh Kumara,Jayakumarb,Balachandranc
experimental part, p. 783 - 788 (2011/05/05)
1,2-Diphenylethyl chloride undergoes solvolysis by SN1 mechanism in aqueous organic solvents. The α-phenyl group of 1,2-diphenylethyl chloride enters into conjugation with the developing carbocationic centre. The β-phenyl group on the other hand was unable to extend its conjugation via neighbouring group participation due to steric inhibition of resonance in the formation of non-classical carbocation. 1,2-Diphenylethyl chloride thus behaves similar to 1-phenylethyl chloride in its solvolysis pattern. The solvolytic rate studies of chloride and methanesulphonate of 1,2-diphenylethyl alcohol in various aqueous organic solvents show that the dispersion observed in the Winstein- Grunwald plot is not due to a change in leaving group but due to the difference in solvation requirements of aromatic and aliphatic groups. Copyright
