24909-60-2 Usage
Uses
Used in Pharmaceutical and Biotechnology Industries:
(3beta)-cholest-5-en-3-yl 4-[(E)-phenyldiazenyl]benzoate is utilized as a research compound in the pharmaceutical and biotechnology sectors. Its distinctive structure allows it to be explored for potential applications in the development of new drugs, as well as serving as a diagnostic tool in the medical field. (3beta)-cholest-5-en-3-yl 4-[(E)-phenyldiazenyl]benzoate's properties make it a promising candidate for further investigation and utilization in advancing healthcare solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 24909-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,0 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24909-60:
(7*2)+(6*4)+(5*9)+(4*0)+(3*9)+(2*6)+(1*0)=122
122 % 10 = 2
So 24909-60-2 is a valid CAS Registry Number.
24909-60-2Relevant academic research and scientific papers
Thermal Properties of Cholesteryl and β-Sitosteryl Esters: The Effect of the Rigid Core on the Thermal Stabilities of Cholesteric and Smectic A Phases
Takenaka, Shunsuke,Koden, Mitsuhiro,Kusabayashi, Shigekazu
, p. 666 - 671 (2007/10/02)
The effect of a central linkage X on the thermal stabilities of the cholesteric and smectic A phases of cholesteryl and β-sitosteryl esters of 4-aryl-X-benzoic and 4-aryl-X-cyclohexanecarboxylic acids (X=-COO-, -CH=N-, -N=N-, -CO-, etc.) has been examined.In both series, the cholesteric-isotropic and smectic A-cholesteric transition temperatures and the transition enthalpies are discussed in terms of the molecular structures and also the angular correlation parameter J22 of the carboxy functions.The transition enthalpies for the smectic A-cholesteric transition are also discussed in terms of the McMillan theory.
