7444-53-3 Usage
Uses
Used in Pharmaceutical Industry:
Ubiquinone Q6 is used as a therapeutic agent for the treatment of heart disease, cancer, and neurodegenerative disorders. Its potential health benefits are attributed to its role in cellular respiration and its antioxidant properties, which may help protect cells from damage and support overall health.
Used in Dietary Supplements:
Ubiquinone Q6 is used as a dietary supplement to support energy production and maintain healthy cellular function. It can be taken orally to help replenish levels of this essential molecule in the body, particularly for individuals who may have difficulty obtaining adequate amounts through their diet alone.
Used in Food Industry:
Ubiquinone Q6 is found in various foods such as meat, fish, and spinach, contributing to the overall nutritional value of these food sources. Its presence in these foods may help support energy production and protect cells from oxidative stress, promoting overall health and well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 7444-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,4 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7444-53:
(6*7)+(5*4)+(4*4)+(3*4)+(2*5)+(1*3)=103
103 % 10 = 3
So 7444-53-3 is a valid CAS Registry Number.
7444-53-3Relevant academic research and scientific papers
A convergent approach to coenzyme Q
Lipshutz, Bruce H.,Bulow, Gerd,Fernandez-Lazaro, Fernando,Kim, Sung-Kyu,Lowe, Richard,Mollard, Paul,Stevens, Kirk L.
, p. 11664 - 11673 (2007/10/03)
Syntheses of coenzyme Q3-8 are described, as well as related systems such as plastoquinone-5. Preparation of the higher homologues of the ubiquinones relies on two new conjunctive reagents, or "linchpins", each of which ultimately corresponds to two or three prenyl units. These allow for attachment of a polyprenyl halide at one end, followed by a Ni(0)-catalyzed cross-coupling at the other terminus with a chloromethylated p-quinone.
