516-89-2 Usage
Uses
Used in Pharmaceutical Industry:
(22E,24R)-24-Methyl-5α-cholesta-6,8(14),22-trien-3β-ol is used as a bioactive compound for its potential health benefits. Its ability to influence cellular function and regulate lipid metabolism may contribute to the development of pharmaceutical products.
Used in Food Industry:
(22E,24R)-24-Methyl-5α-cholesta-6,8(14),22-trien-3β-ol is used as a functional ingredient in the food industry. Its potential to modulate immune response and its presence in plants may contribute to the development of health-promoting food products.
Further research on (22E,24R)-24-Methyl-5α-cholesta-6,8(14),22-trien-3β-ol may provide valuable insights into its potential health benefits and industrial uses, expanding its applications in both the pharmaceutical and food industries.
Check Digit Verification of cas no
The CAS Registry Mumber 516-89-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 516-89:
(5*5)+(4*1)+(3*6)+(2*8)+(1*9)=72
72 % 10 = 2
So 516-89-2 is a valid CAS Registry Number.
516-89-2Relevant academic research and scientific papers
REGIOCONTROLLED SYNTHESIS OF THE ERGOSTEROL B-ISOMERS
Dolle, Roland E.,Schmidt, Stanley J.,Kruse, Lawrence I.
, p. 1581 - 1582 (2007/10/02)
A novel, regiocontrolled synthesis of the ergosterol B-isomers, (1), (2) and (3) is described, the success of which was realized via the highly regioselective formation of intermediate trienoltriflates, (7), (8) and (9).
Structure and Chemistry of ?-Allyl Palladium Complexes from Steroids
Mahe, Christian,Patin, Henri,Hulle, Marie-Therese Van,Barton, Derek H.R.
, p. 2504 - 2508 (2007/10/02)
The synthesis and structures of ?-allyl palladium complexes prepared from vitamins D2 and D3 and from ergosterol, 7,8-didehydrocholesterol, and 3-epi-cholesterol are described.The mechanism of palladisation is descussed as well as the transformation of the complexes into conjugated trienes or allylic alcohols.
