69251-08-7 Usage
Uses
Used in Pharmaceutical Industry:
(2E,4E,6E)-3-methyl-7-(1,1,3,3-tetramethyl-2,3-dihydro-1H-inden-5-yl)octa-2,4,6-trienoic acid is used as a pharmaceutical agent for its potential bioactivity and antioxidant properties. It can be employed in the development of treatments and therapies that promote health and well-being.
Used in Food Industry:
As a natural food coloring agent, (2E,4E,6E)-3-methyl-7-(1,1,3,3-tetramethyl-2,3-dihydro-1H-inden-5-yl)octa-2,4,6-trienoic acid is used in the food industry to provide color and enhance the visual appeal of various food products. Its natural origin makes it a preferred choice over synthetic coloring agents.
Used in Cosmetic Industry:
(2E,4E,6E)-3-methyl-7-(1,1,3,3-tetramethyl-2,3-dihydro-1H-inden-5-yl)octa-2,4,6-trienoic acid is used in the cosmetic industry for its antioxidant properties, which can help protect the skin from oxidative stress and promote a healthy appearance. Its natural origin also makes it an attractive ingredient for cosmetic products that emphasize natural and healthy ingredients.
Check Digit Verification of cas no
The CAS Registry Mumber 69251-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,5 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69251-08:
(7*6)+(6*9)+(5*2)+(4*5)+(3*1)+(2*0)+(1*8)=137
137 % 10 = 7
So 69251-08-7 is a valid CAS Registry Number.
69251-08-7Relevant academic research and scientific papers
Arotinoids, a new class of highly active retinoids
Loeliger,Bollag,Mayer
, p. 9 - 15 (2007/10/02)
The synthesis and biological activity of new aromatic retinoids are reported. The most active ones belong to a chemical class of compounds, which we have termed 'arotinoids'. For the compound p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-propenyl)]-benzoic acid ethyl ester, a therapeutic potency in the antipapilloma test was found which exceeds that of retinoic acid by a factor of 8000, while the concurrently observed toxic hypervitaminosis A effects are only increased by a factor of 800. The structural relationship of the arotinoids with retinoic acid is demonstrated; the arotinoids contain the retinoic acid carbon skeleton in a fixed cisoid geometric conformation.
