25612-59-3 Usage
Uses
Used in Anticancer Applications:
Tocotrienol, delta is used as an anticancer agent for inhibiting the growth of human breast cancer cells. Its antioxidant properties contribute to its potential role in cancer prevention and treatment.
Used in Antioxidant Applications:
Tocotrienol, delta is used as an antioxidant in various industries, such as the pharmaceutical and dietary supplement industries, to protect cells from oxidative damage and maintain overall health.
Used in Pharmaceutical Industry:
Tocotrienol, delta is used as a pharmaceutical agent for its potential therapeutic benefits, including its antioxidant and anticancer properties, which can be utilized in the development of new drugs and treatments for various health conditions.
Used in Dietary Supplements:
Tocotrienol, delta is used as an ingredient in dietary supplements for its health-promoting properties, such as its antioxidant and potential cancer-fighting capabilities, contributing to overall well-being and health maintenance.
Check Digit Verification of cas no
The CAS Registry Mumber 25612-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,1 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25612-59:
(7*2)+(6*5)+(5*6)+(4*1)+(3*2)+(2*5)+(1*9)=103
103 % 10 = 3
So 25612-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C27H40O2/c1-20(2)10-7-11-21(3)12-8-13-22(4)14-9-16-27(6)17-15-24-19-25(28)18-23(5)26(24)29-27/h10,12,14,18-19,28H,7-9,11,13,15-17H2,1-6H3/b21-12+,22-14+/t27-/m1/s1
25612-59-3Relevant 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.
