557794-36-2 Usage
Description
4,4'-DI-N-ACETYLAMINO-DIPHENYLSULFOXIDE-D8 is an isotopically labeled intermediate of Dapsone, which is a chemical compound with a greyish-white solid appearance. It is characterized by its unique molecular structure and properties, making it a valuable compound for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
4,4'-DI-N-ACETYLAMINO-DIPHENYLSULFOXIDE-D8 is used as an isotopically labeled intermediate for Dapsone, a drug with various therapeutic applications. The incorporation of deuterium (D8) in its structure allows for enhanced stability and improved understanding of the compound's behavior in biological systems.
Used in Research and Development:
In the field of research and development, 4,4'-DI-N-ACETYLAMINO-DIPHENYLSULFOXIDE-D8 serves as a valuable tool for studying the properties and interactions of Dapsone and its derivatives. The isotopically labeled compound can be used to investigate the mechanisms of action, metabolic pathways, and potential side effects of Dapsone, leading to the development of more effective and safer therapeutic agents.
Used in Quality Control and Analytical Chemistry:
4,4'-DI-N-ACETYLAMINO-DIPHENYLSULFOXIDE-D8 can be employed as a reference material or internal standard in quality control and analytical chemistry. Its isotopically labeled nature makes it an ideal candidate for accurate quantification and identification of Dapsone and related compounds in various samples, including pharmaceutical formulations, biological fluids, and environmental matrices.
Used in Drug Metabolism and Pharmacokinetic Studies:
The isotopically labeled intermediate of Dapsone, 4,4'-DI-N-ACETYLAMINO-DIPHENYLSULFOXIDE-D8, can be utilized in drug metabolism and pharmacokinetic studies to better understand the absorption, distribution, metabolism, and excretion of Dapsone in the body. This information is crucial for optimizing the drug's dosage, formulation, and administration, as well as for assessing its safety and efficacy in clinical settings.
Check Digit Verification of cas no
The CAS Registry Mumber 557794-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,7,7,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 557794-36:
(8*5)+(7*5)+(6*7)+(5*7)+(4*9)+(3*4)+(2*3)+(1*6)=212
212 % 10 = 2
So 557794-36-2 is a valid CAS Registry Number.
557794-36-2Relevant articles and documents
Phenylene ring motions in isomeric glassy epoxy networks and their contributions to thermal and mechanical properties
Tu, Jianwei,Tucker, Samuel J.,Christensen, Stephen,Sayed, Abdelwahed R.,Jarrett, William L.,Wiggins, Jeffrey S.
, p. 1748 - 1758 (2015/03/31)
Cross-linked epoxies prepared from diglycidyl ether of bisphenol A (DGEBA) exhibit substantial property differences due to isomeric structures of the diamine curatives, 3,3′- and 4,4′-diaminodiphenyl sulfone (DDS). Here, the motions of phenylene rings on both the bisphenol A (BPA) and DDS structures of the networks were investigated through solid-state NMR 2H line shape analysis to trace the molecular origins. Ring deuterated monomers, namely, DGEBA-d8, 33DDS-d8, and 44DDS-d8, were synthesized, and four deuterated networks were prepared. The line shapes of the ring motions were interpreted using a motional model that described both ring π-flips and main-chain fluctuations. The contributions of different ring motions to mechanical relaxations are elucidated, and the molecular origins of property differences are identified.
