78451-64-6 Usage
Uses
Used in Pharmaceutical Industry:
2-(benzylamino)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one is used as an intermediate in the synthesis of pharmaceuticals for its antimicrobial and anticancer properties. It plays a crucial role in the development of new drugs that can target various diseases and conditions.
Used in Organic Compounds Synthesis:
2-(benzylamino)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one is used as an intermediate in the synthesis of organic compounds, contributing to the creation of a wide range of chemical products with diverse applications in various industries.
Used in Anticancer Applications:
2-(benzylamino)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one is used as a potential anticancer agent, as it has been studied for its ability to target and inhibit the growth of cancer cells. Its antimicrobial properties also contribute to its potential use in cancer treatment, as infections are a common complication in cancer patients.
Used in Drug Development:
2-(benzylamino)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one is used in drug development as a promising candidate for the creation of new therapeutic agents. Its unique chemical structure and properties make it a valuable component in the design and synthesis of novel drugs with potential applications in various medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 78451-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,5 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78451-64:
(7*7)+(6*8)+(5*4)+(4*5)+(3*1)+(2*6)+(1*4)=156
156 % 10 = 6
So 78451-64-6 is a valid CAS Registry Number.
78451-64-6Relevant academic research and scientific papers
Reaction of 5,5-diphenyl-2-thiohydantoin with ethyl chloroacetate: Synthesis and crystal and molecular structure of 2,3,5,6-tetrahydroimidazo--thiazol-3,6-dione
Kiec-Kononowich, Katarzyna,Karolak-Wojciechowska, Janina,Kwiatkowskii, Witold
, p. 563 - 574 (2007/10/02)
The crystal and molecular structure of the title compound, obtained as a result of intramolecular cyclization of 5,5-diphenyl-2-carboxymethylmercaptohydantoin, has been determined from X-ray diffractometer data.The final R was 0.049 for 1869 reflections.T
SYNTHESES OF SOME 2-AMINO-5,5-DIPHENYLIMIDAZOLIN-4-ONE DERIVATIVES
Kiec-Kononowicz, Katarzyna,Zejc, Alfred
, p. 2217 - 2224 (2007/10/02)
Derivatives of 2-amino-5,5-diphenylimidazolin-4-one were obtained in a thermal reaction of 5,5-diphenyl-2-thiohydantoin with primary or secondary amines.Such compounds can be obtained also in the reaction of 2-ethylthiohydantoin with the above mentioned amines.Preliminary pharmacological testing of compound 7 for cardiovascular activity has been performed.
