65377-86-8 Usage
Uses
Used in Dietary Supplements:
Ersterol is used as a dietary supplement for its vitamin D2 content, which supports overall health and wellness. It helps in maintaining adequate levels of vitamin D in the body, contributing to bone health and immune function.
Used in Pharmaceutical Applications:
Ersterol is being investigated for its potential as a therapeutic agent in the treatment of various conditions. Its anti-inflammatory and antioxidant properties make it a promising candidate for managing inflammation-related disorders. Additionally, research is exploring its role in cancer therapy and infectious disease treatment, given its potential to modulate immune responses and target specific cellular pathways.
Used in Nutraceutical Industry:
In the nutraceutical industry, ersterol is utilized for its health-promoting properties. It is incorporated into products that aim to enhance bone health, support the immune system, and provide antioxidant benefits. Its role in cell membrane synthesis also makes it a valuable ingredient in formulations designed to support skin health and integrity.
Used in Research and Development:
Ersterol is a key compound in scientific research, particularly in the fields of biochemistry, cell biology, and pharmacology. It is used in laboratory settings to study the mechanisms of action related to its health benefits and therapeutic potential. Researchers are also exploring methods to enhance the bioavailability and efficacy of ersterol for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 65377-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,7 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65377-86:
(7*6)+(6*5)+(5*3)+(4*7)+(3*7)+(2*8)+(1*6)=158
158 % 10 = 8
So 65377-86-8 is a valid CAS Registry Number.
65377-86-8Relevant academic research and scientific papers
Hydrotitanation-Protonation of Vitamin D2 and Its Analogues: An Efficient Method for the Preparation of 10,19-Dihydrovitamins D2 Including Dihydrotachysterol2
Cota, J. G.,Meilan, M. C.,Mourino, A.,Castedo, L.
, p. 6094 - 6099 (2007/10/02)
In this study we describe an easy and efficient method for the preparation of the known 10,19-dihydrovitamins D2 2b (DHV2-II), 2c (DHV2-IV), 3c (dihydrotachysterol2, DHT2), and the new dihydrovitamins D2 2f and 2g.This method is based on the regioselective hydrometalation reaction of vitamin D2 and its derivatives with the system Cp2TiCl2-LiAlH4 or Cp2TiCl2-Red-Al (Aldrich).Under optimal conditions, the reaction with the former of these hydrometalating systems takes place with a high degree of stereoselectivity and allows labelling at C-19.
