19953-93-6 Usage
Uses
Used in Antioxidant Applications:
Phytol is used as an antioxidant, which helps to protect cells from damage caused by free radicals and oxidative stress. Its antioxidant properties make it a promising candidate for various health and wellness applications.
Used in Anticancer Applications:
Phytol is used as an anticancer agent, which has been studied for its potential to inhibit the growth and proliferation of cancer cells. Its anticancer properties make it a promising candidate for cancer prevention and treatment.
Used in Lipid Metabolism:
Phytol is used in lipid metabolism, where it plays a role in the regulation of lipid synthesis and breakdown. Its involvement in lipid metabolism makes it a potential candidate for the development of treatments for metabolic disorders and obesity.
Used in Immune System Modulation:
Phytol is used in immune system modulation, where it has been shown to modulate the immune response and enhance the body's ability to fight infections and diseases. Its immune-modulating properties make it a promising candidate for the development of treatments for immune-related disorders.
Used in Fragrances:
Phytol is used as a fragrance ingredient in the perfumery industry, where it adds a unique and pleasant scent to various products.
Used in Flavoring Agents:
Phytol is used as a flavoring agent in the food industry, where it imparts a distinct and desirable taste to various food products.
Check Digit Verification of cas no
The CAS Registry Mumber 19953-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,5 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19953-93:
(7*1)+(6*9)+(5*9)+(4*5)+(3*3)+(2*9)+(1*3)=156
156 % 10 = 6
So 19953-93-6 is a valid CAS Registry Number.
19953-93-6Relevant academic research and scientific papers
Sulphone-based Elimination Reactions in Synthesis. Part 1. Moenocinol
Kocienski, Philip,Todd, Michael
, p. 1777 - 1781 (2007/10/02)
The fluoride-induced elimination of a β-phenylsulphonylsilane and the reductive elimination of a β-oxysulphone are key olefin-forming reactions in a synthesis of moenocinol .
A Synthesis of Moenocinol
Kocienski, Philip J.
, p. 2037 - 2039 (2007/10/02)
The fluoride-induced elimination of a β-silyl sulfone and the reductive elimination of a β-acyloxy sulfone are key olefin-forming reactions in a new synthesis of moenocinol .
