50305-81-2 Usage
Description
Cholesterol trans-cinnamate is a derivative of cholesterol, a common sterol found in cell membranes and animal tissues. It is produced by esterification of cholesterol with trans-cinnamic acid, a natural compound found in plants. CHOLESTEROL TRANS-CINNAMATE has been studied for its potential use in pharmaceutical and cosmetic applications due to its antioxidant, anti-inflammatory, and anti-cancer properties, making it an attractive candidate for development in these fields. Furthermore, it has shown potential in enhancing the stability and bioavailability of certain drugs.
Uses
Used in Pharmaceutical Applications:
Cholesterol trans-cinnamate is used as a pharmaceutical agent for its antioxidant, anti-inflammatory, and anti-cancer properties. It has the potential to be developed into treatments for various diseases and conditions, particularly those involving oxidative stress and inflammation.
Used in Cosmetic Applications:
In the cosmetic industry, cholesterol trans-cinnamate is used as an ingredient in skincare and beauty products for its antioxidant and anti-inflammatory properties. It may help to protect the skin from environmental damage, reduce inflammation, and promote a healthier appearance.
Used in Drug Delivery Systems:
Cholesterol trans-cinnamate has shown potential in enhancing the stability and bioavailability of certain drugs. It can be used as a component in drug delivery systems to improve the effectiveness and safety of medications, particularly in the development of novel pharmaceutical formulations.
Used in Research and Development:
Cholesterol trans-cinnamate is also used in research and development for its potential benefits and applications in various industries. Ongoing studies aim to further explore its properties and identify new uses for this compound, expanding its potential impact on healthcare, cosmetics, and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 50305-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,0 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50305-81:
(7*5)+(6*0)+(5*3)+(4*0)+(3*5)+(2*8)+(1*1)=82
82 % 10 = 2
So 50305-81-2 is a valid CAS Registry Number.
50305-81-2Relevant articles and documents
Mizoroki-Heck Reaction of Unstrained Aryl Ketones via Ligand-Promoted C-C Bond Olefination
Wang, Mei-Ling,Xu, Hui,Li, Han-Yuan,Ma, Biao,Wang, Zhen-Yu,Wang, Xing,Dai, Hui-Xiong
, p. 2147 - 2152 (2021/04/05)
Mizoroki-Heck reaction of unstrained aryl ketone with acrylate/styrene is accomplished via palladium-catalyzed ligand-promoted C-C bond cleavage. Various (hetero)aryl ketones are compatible in the reaction, affording the alkene product in good to excellent yields. Further applications in the late-stage olefination of some drugs, natural products, and fragrance-derived aryl ketones demonstrate the synthetic utility of this protocol. By employing ketone as both the directing group and the leaving group, 1,2-bifunctionalization is achieved via sequential ortho-C-H alkylation/ipso-Heck olefination.
SYNTHESIS AND PROPERTIES OF LIQUID CRYSTALS. III. CHOLESTERYL ESTERS OF SOME CIS,TRANS-ISOMERIC UNSATURATED ACIDS
Bogat-skii, A. V.,Galantina, A. I.,Derkach, L. G.,Taubert D.
, p. 2072 - 2075 (2007/10/02)
A series of esters of cholesterol with the cis,trans isomers of unsaturated monocarboxylic acids were synthesized.The effect of the nature and of the configuration of the substituents in relation to the double bond in the acid component of the cholesterol esters on the mesogenic capacity was established.The phase transition temperatures were determined.
