82263-61-4 Usage
Uses
Used in Pharmaceutical Applications:
(5Z,8Z,10E,12E,14R,15S)-14,15-dihydroxyicosa-5,8,10,12-tetraenoic acid is used as an anti-inflammatory agent for its ability to reduce inflammation and promote overall health. Its presence in the human diet is crucial for maintaining a balanced immune response and supporting various biological processes.
Used in Nutritional Supplements:
In the Nutritional Supplements Industry, (5Z,8Z,10E,12E,14R,15S)-14,15-dihydroxyicosa-5,8,10,12-tetraenoic acid is used as an essential nutrient to support brain function, cardiovascular health, and immune system regulation. Its inclusion in supplements helps ensure that individuals who may not get enough of this nutrient from their diet can still receive its health benefits.
Used in Research and Development:
(5Z,8Z,10E,12E,14R,15S)-14,15-dihydroxyicosa-5,8,10,12-tetraenoic acid is used as a key compound in research and development for its potential applications in various fields, including pharmaceuticals, nutraceuticals, and functional foods. Its unique chemical structure and properties make it an interesting target for scientists exploring new therapeutic approaches and health-promoting products.
Check Digit Verification of cas no
The CAS Registry Mumber 82263-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,6 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82263-61:
(7*8)+(6*2)+(5*2)+(4*6)+(3*3)+(2*6)+(1*1)=124
124 % 10 = 4
So 82263-61-4 is a valid CAS Registry Number.
82263-61-4Relevant academic research and scientific papers
Stereoselective ozonolysis of TMS-substituted allylic alcohol derivatives and synthesis of 14R,15 S - And 14 S,15 S-diHETE
Saito, Shun,Yamazaki, Takashi,Kobayashi, Yuichi
, p. 7636 - 7647 (2018/11/02)
Ozonolysis of TMS-substituted olefins produces α-carbonyl TMS peroxides without cleavage of the CC bond. Herein, stereochemistry in the ozonolysis was studied using silyl derivatives of (E)- and (Z)-(1-TMS)alk-1-en-3-ols. The (E)-isomers afforded the anti-3-siloxy-2-(TMS-oxy)aldehydes as the major stereoisomer (anti/syn = 3-9:1) after reductive work-up with Ph3P. In contrast, Z-olefins selectively gave the syn isomers with syn/anti ratios of 4-19:1. Facial selection was speculated based on the Cieplak effect. This ozonolysis was successfully applied for the synthesis of 14R,15S- and 14S,15S-diHETEs (anti and syn isomers, respectively) in enantioenriched forms.
ON THE SYNTHESIS AND STRUCTURE OF LIPOXIN B
Corey, E. J.,Mehrotra, Mukund M.,Su, Wei-guo
, p. 1919 - 1922 (2007/10/02)
A synthesis of lipoxin B, a recently discovered biologically active eicosanoid, and the assignment of stereoformula 2 is reported.
