1200446-88-3 Usage
Uses
Used in Pharmaceutical Applications:
(3S)-β-Cryptoxanthin is used as an antioxidant for preventing free radical damage to cells and DNA. Its antioxidant properties help protect the body from oxidative stress and reduce the risk of various diseases.
Used in Anticancer Applications:
(3S)-β-Cryptoxanthin is used as a chemopreventative agent, particularly against lung cancer. It has shown potential in reducing the risk of developing lung cancer by neutralizing harmful free radicals and preventing damage to the DNA of lung cells.
Used in Nutritional Supplements:
(3S)-β-Cryptoxanthin is used as a nutritional supplement to support overall health and well-being. Its antioxidant properties can help improve the immune system and promote a healthy lifestyle.
Used in Food Industry:
(3S)-β-Cryptoxanthin is used as a natural colorant in the food industry to provide a vibrant hue to various products. Its antioxidant properties also contribute to the preservation and shelf life of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 1200446-88-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,0,4,4 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1200446-88:
(9*1)+(8*2)+(7*0)+(6*0)+(5*4)+(4*4)+(3*6)+(2*8)+(1*8)=103
103 % 10 = 3
So 1200446-88-3 is a valid CAS Registry Number.
1200446-88-3Relevant academic research and scientific papers
Synthesis of (3S)- and (3R)-3-hydroxy-β-ionone and their transformation into (3S)- and (3R)-β- cryptoxanthin
Khachik, Frederick,Chang, An-Ni
, p. 509 - 516 (2011/04/16)
(3S)- and (3R)-3-Hydroxy-β-ionone and (3S)- and (3R)-3-Hydroxy-β- ionone synthesized in high enantiomeric purity from commercially available () - ionone. These ionones were then transformed into (3R) - cryptoxanthin and (3S) - cryptoxanthin by a C15+C10+C15 Wittig coupling strategy according to known methods. This methodology can considerably simplify the total synthesis of optically active carotenoids with 3-hydroxy - end groups that possess significant biological activities. Georg Thieme Verlag Stuttgart New York.
