56112-66-4 Usage
Uses
Used in Pharmaceutical Industry:
5-[(E)-phenyldiazenyl]pyrimidine-2,4,6(1H,3H,5H)-trione is used as an intermediate in the synthesis of various drugs and pharmaceuticals. Its unique chemical structure allows it to be a valuable component in the development of new medications.
Used in Antimicrobial Applications:
5-[(E)-phenyldiazenyl]pyrimidine-2,4,6(1H,3H,5H)-trione is studied for its potential antimicrobial properties, which can be utilized in the development of new antimicrobial agents to combat resistant bacteria and other pathogens.
Used in Antioxidant Applications:
5-[(E)-phenyldiazenyl]pyrimidine-2,4,6(1H,3H,5H)-trione has been studied for its potential antioxidant properties, making it a candidate for use in the development of antioxidants that can protect cells from oxidative damage and potentially reduce the risk of various diseases.
Used in Anti-inflammatory Applications:
5-[(E)-phenyldiazenyl]pyrimidine-2,4,6(1H,3H,5H)-trione is also being investigated for its potential anti-inflammatory properties, which could be applied in the development of new treatments for inflammatory conditions.
Used in Materials Science and Organic Synthesis:
Due to its unique chemical structure and properties, 5-[(E)-phenyldiazenyl]pyrimidine-2,4,6(1H,3H,5H)-trione may have potential applications in the field of materials science and organic synthesis, where it could be used to create new materials or facilitate chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 56112-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,1 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56112-66:
(7*5)+(6*6)+(5*1)+(4*1)+(3*2)+(2*6)+(1*6)=104
104 % 10 = 4
So 56112-66-4 is a valid CAS Registry Number.
56112-66-4Relevant academic research and scientific papers
Ahmed, Mahmoud Moursy,Masoud, Mamdouh Saad,Sweyllam, Amr Mohamed
, (2020)
A group of biologically active ligands: 5-(2hydroxyphenylide) barbituric acid (L1), 5-(phenyl azo) thiobarbituric acid (L2) and 5-(phenyl azo) barbituric acid (L3) and its complexes with Os(VIII), Ru(III),Zr(IV) and V(III)
Dissociation constants of substituted aryl azo barbituric and thiobarbituric acids
Masoud, Mamdouh S.,Ghonaim, Ahmed K.,Ahmed, Rabah H.,Mahmoud, Ahmed A.,Ali, Alaa E.
, p. 531 - 542 (2007/10/03)
The acid dissociation constants of 5-(substituted phenylazo) barbituric and thiobarbituric acids were determined in aqueous media and in 25%-75% (v/v) ethanol-water and dioxanewater mixtures potentiometrically in the temperature range 25-40°C, in presence
