612480-60-1 Usage
Uses
Used in Analytical Chemistry:
4,4'-Dihydroxydiphenyl-D8 (RINGS-D8) is used as an internal standard in analytical chemistry for the quantification and identification of related compounds. The incorporation of deuterium atoms allows for improved signal-to-noise ratios and reduced interference from background signals, leading to more accurate and reliable results.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4,4'-Dihydroxydiphenyl-D8 (RINGS-D8) serves as a valuable research tool for studying the metabolism, pharmacokinetics, and pharmacodynamics of drugs containing similar structures. The deuterium labeling can help differentiate the compound of interest from its metabolites and other endogenous substances, providing insights into drug action and potential side effects.
Used in Environmental Studies:
4,4'-Dihydroxydiphenyl-D8 (RINGS-D8) can be employed in environmental studies to track the fate and transport of pollutants with similar chemical structures. The deuterium labeling allows for the detection and quantification of these pollutants in complex environmental samples, aiding in the assessment of their impact on ecosystems and human health.
Used in Material Science:
In material science, 4,4'-Dihydroxydiphenyl-D8 (RINGS-D8) can be utilized to investigate the properties and behavior of materials containing similar structures. The deuterium labeling can provide insights into the molecular interactions, stability, and performance of these materials, contributing to the development of new and improved materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 612480-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,2,4,8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 612480-60:
(8*6)+(7*1)+(6*2)+(5*4)+(4*8)+(3*0)+(2*6)+(1*0)=131
131 % 10 = 1
So 612480-60-1 is a valid CAS Registry Number.
612480-60-1Relevant academic research and scientific papers
Catalano, Donata,Chiezzi, Leonardo,Domenici, Valentina,Geppi, Marco,Veracini, Carlo Alberto
, p. 10104 - 10113 (2003)
In this work, a new procedure for the synthesis of the selectivity deuterium-labeled chiral liquid crystal (+)-(S)-4-[4′-(1-methylheptyloxy)] biphenyl 4(10-undecenylox)benzoate (11EB1M7) has been developed, aimed to the study of its structure, orientational ordering, and dynamic behavior by means of 2H NMR. 11EB1M7 was investigated throughout its mesophasic range, formed by a very rich variety of chiral liquid crystalline phases including blue, cholesteric, TGBA*, and smectic C*. Two isotopomers were synthesized by labeling 11EB1M7 on either the phenyl or the biphenyl moiety of the mesogenic core. This allowed structural information (such as the tilt angle of the rigid fragments of the molecule and the angle between their para axes), orientational order parameters, and individual diffusional coefficients for the various overall and internal motions to be obtained from 2H NMR spectra and relaxation measurements by applying suitable data analyses based on several theoretical models.
