61254-28-2 Usage
Description
(4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-5-(4-methylphenyl)-2-phenyl-2,4-dihydro-3H-pyrazol-3-one is a complex organic molecule with a pyrazolone core structure. It features an aziridine ring, a methylsulfanyl group, a phenyl group, and a methylphenyl substituent. (4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-5-(4-methylphenyl)-2-phenyl-2,4-dihydro-3H-pyrazol-3-one is a potential antineoplastic agent, which has been studied for its ability to induce DNA damage and apoptosis in cancer cells. Additionally, it has been investigated for its potential use in photodynamic therapy for cancer treatment. Due to its intricate structure and potential biological activity, this compound holds significant interest for further research and development in medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
(4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-5-(4-methylphenyl)-2-phenyl-2,4-dihydro-3H-pyrazol-3-one is used as a potential antineoplastic agent for its ability to induce DNA damage and apoptosis in cancer cells. This characteristic makes it a promising candidate for the development of new cancer treatments.
Used in Photodynamic Therapy:
In the field of photodynamic therapy, (4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-5-(4-methylphenyl)-2-phenyl-2,4-dihydro-3H-pyrazol-3-one is used as a potential therapeutic agent. Its investigation in this area aims to leverage its properties to enhance the effectiveness of cancer treatment through photodynamic therapy, which combines the use of light with photosensitizing agents to target and destroy cancer cells.
Used in Medicinal Chemistry Research:
(4E)-4-[aziridin-1-yl(methylsulfanyl)methylidene]-5-(4-methylphenyl)-2-phenyl-2,4-dihydro-3H-pyrazol-3-one is also used in the field of medicinal chemistry research for its potential to contribute to the development of novel cancer therapies. Its complex structure and biological activity make it an interesting subject for further study, with the goal of understanding its mechanisms of action and optimizing its properties for therapeutic use.
Check Digit Verification of cas no
The CAS Registry Mumber 61254-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,5 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61254-28:
(7*6)+(6*1)+(5*2)+(4*5)+(3*4)+(2*2)+(1*8)=102
102 % 10 = 2
So 61254-28-2 is a valid CAS Registry Number.
61254-28-2Relevant articles and documents
Reaction of Ketene Dithioacetals with Aziridine. A New Synthesis of N-Vinylaziridines and their Iodide Ion-assisted Rearrangement to Pyrrolines
Basaveswara Rao,Suresh,Kumar, Arvind,Ila,Junjappa
, p. 955 - 960 (2007/10/03)
The ketene dithioacetals 1, 4, 9 and 11 react readily with aziridine 2 to give the corresponding N-vinylaziridines 3, 5, 8 and 12 respectively, which on iodide ion-catalyzed rearrangement undergo ring expansion to give pyrrolines 14, 18, 21 and 22 respect
