6372-58-3 Usage
Uses
Used in Pharmaceutical Industry:
(1-benzyl-3-phenylaziridin-2-yl)(4-methylphenyl)methanone is used as a potential pharmaceutical compound for its possible medicinal or biological properties. The benzyl and phenylaziridin-2-yl groups are commonly found in pharmaceuticals, indicating that this chemical may have therapeutic applications that require further research and development.
Used in Organic Synthesis:
(1-benzyl-3-phenylaziridin-2-yl)(4-methylphenyl)methanone is also used as a building block or intermediate in organic synthesis due to the presence of the methanone group. Its structural complexity and the variety of attached groups make it a candidate for creating more complex molecules or for use in the synthesis of other organic compounds.
Further research and characterization are necessary to fully understand the properties and potential applications of (1-benzyl-3-phenylaziridin-2-yl)(4-methylphenyl)methanone, as its diverse composition suggests a wide range of possibilities across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6372-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,7 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6372-58:
(6*6)+(5*3)+(4*7)+(3*2)+(2*5)+(1*8)=103
103 % 10 = 3
So 6372-58-3 is a valid CAS Registry Number.
6372-58-3Relevant academic research and scientific papers
I2/TBHP mediated diastereoselective synthesis of spiroaziridines
Ashitha, Kizhakkan Thiruthi,Vinaya, Puthiya Purayil,Krishna, Ajay,Vincent, Deepthy Cheeran,Jalaja, Renjitha,Varughese, Sunil,Somappa, Sasidhar Balappa
supporting information, p. 1588 - 1593 (2020/03/06)
Eventhough spiroheterocycles are considered as emerging drug candidates, synthesis of spiroaziridines has not been well explored so far. Herein, we disclose an efficient I2/TBHP mediated diastereoselective synthesis of N-alkyl spiroaziridines from primary amines and easily accessible α,β-unsaturated ketones. The reaction is also compatible for the synthesis of 2-aroylaziridines.
