76686-31-2 Usage
Uses
Used in Pharmaceutical Industry:
[(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride is used as an active pharmaceutical ingredient for its antioxidant properties, which can contribute to the development of therapeutic products.
Used in Drug Delivery Systems:
In the field of drug delivery, [(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride is used as a component in lipid-based drug delivery systems. Its unique structure with a hydrophobic tail and a hydrophilic head group allows for efficient encapsulation and targeted delivery of therapeutic agents.
Used in Biotechnology:
Within the biotechnology industry, [(2E,4E)-(R)-5-(4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-3-methyl-2,4-pentadienyl]-triphenylphosphonium chloride is utilized as a key compound in the development of novel pharmaceutical products, taking advantage of its antioxidant properties and potential for therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 76686-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,8 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76686-31:
(7*7)+(6*6)+(5*6)+(4*8)+(3*6)+(2*3)+(1*1)=172
172 % 10 = 2
So 76686-31-2 is a valid CAS Registry Number.
76686-31-2Relevant 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.
Ethynylcyclohexene compounds
-
, (2008/06/13)
A process for the manufacture of compounds of the general formula STR1 wherein R1 signifies hydroxy or an etherified hydroxy group, and of zeaxanthin by converting a compound of the general formula STR2 wherein R1 has the above signi
