1175-39-9 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-2,8-dimethyl-2-[(3E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2H-chromen-6-ol is used as a potential pharmaceutical agent for its possible antioxidant and anti-inflammatory properties. Its unique structure may contribute to its effectiveness in treating various conditions, and further research is needed to explore its full potential in this field.
Used in Nutraceutical Industry:
In the nutraceutical industry, (2R)-2,8-dimethyl-2-[(3E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2H-chromen-6-ol may be utilized as a natural antioxidant or anti-inflammatory supplement. Its presence in natural sources could make it a valuable ingredient in health products aimed at promoting overall wellness and combating oxidative stress.
Used in Cosmetic Industry:
(2R)-2,8-dimethyl-2-[(3E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2H-chromen-6-ol could be employed in the cosmetic industry as an ingredient with potential antioxidant and anti-inflammatory benefits. Its lipid-soluble nature may make it suitable for formulations in skincare products designed to protect and nourish the skin.
Used in Research and Development:
In the field of research and development, (2R)-2,8-dimethyl-2-[(3E)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,4-dihydro-2H-chromen-6-ol serves as a subject of study for scientists to investigate its biological activities and potential applications. Understanding its properties and mechanisms of action can lead to the discovery of new therapeutic agents or applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1175-39-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,7 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1175-39:
(6*1)+(5*1)+(4*7)+(3*5)+(2*3)+(1*9)=69
69 % 10 = 9
So 1175-39-9 is a valid CAS Registry Number.
1175-39-9Relevant academic research and scientific papers
SYNTHESIS OF TOCOTRIENOLS FROM O-CRESOL DERIVATIVES
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, (2019/04/11)
The present invention provides an environmentally benign, facile process for preparation of Tocotrienols from commercially available derivatives of o-Cresol.
A short and convenient chemical route to optically pure 2-methyl chromanmethanols. Total asymmetric synthesis of β-, γ-, and δ-tocotrienols
Couladouros, Elias A.,Moutsos, Vassilios I.,Lampropoulou, Maria,Little, James L.,Hyatt, John A.
, p. 6735 - 6741 (2008/02/11)
(Chemical Equation Presented) With use of inexpensive commercially available raw materials, chromanmethanol precursors to the natural β-, γ-, and δ-tocotrienols have been prepared in high yield. Enzymatic resolution afforded chiral chromanmethanols in high enantiomeric excess. Subsequent attachment of the farnesyl side chain was high yielding, thus allowing the preparation of asymmetric β-, γ-, and δ-tocotrienols in one final step wherein simultaneous deprotection of the phenol and removal of the sulfone group occurs. This chemistry provides the first synthesis of natural-series β-tocotrienol.
Constituents of the seeds of Garcinia kola: Two new antioxidants, garcinoic acid and garcinal
Terashima, Kenji,Shimamura, Tomoyuki,Tanabayashi, Miho,Aqil, Mohammad,Akinniyi, John A.,Niwa, Masatake
, p. 1559 - 1566 (2007/10/03)
Two new chromanols, named garcinoic acid and garcinal, were isolated together with a known chromanol, δ-tocotrienol and three known biflavonoids, garcinianin, GB-1 and GB-2, from the seeds of Garcinia kola Heckel (Guttiferae) collected in Nigeria and their structures were characterized on the basis of the spectroscopic and chemical evidence. Garcinoic acid, garcinal and δ-tocotrienol showed about 1.5 times stronger antioxidation activity than that of dl-α-tocopherol.
