19485-76-8 Usage
Uses
Used in the Food Industry:
Cholesteryl elaidate is used as a cholesterol source in the production of various processed foods for [reasons such as enhancing texture, stability, or shelf life]. It is commonly found in margarine, baked goods, and snack foods, where it contributes to the overall cholesterol content of these products.
Used in Research and Development:
Cholesteryl elaidate is also used in scientific research and development for studying the effects of cholesterol on human health and the role of cholesteryl esters in lipid metabolism. This helps in understanding the potential risks and benefits associated with the consumption of cholesteryl elaidate and other similar compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 19485-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19485-76:
(7*1)+(6*9)+(5*4)+(4*8)+(3*5)+(2*7)+(1*6)=148
148 % 10 = 8
So 19485-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C45H78O2/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-25-43(46)47-38-30-32-44(5)37(34-38)26-27-39-41-29-28-40(36(4)24-22-23-35(2)3)45(41,6)33-31-42(39)44/h14-15,26,35-36,38-42H,7-13,16-25,27-34H2,1-6H3/b15-14+/t36-,38+,39+,40-,41+,42+,44+,45-/m1/s1
19485-76-8Relevant academic research and scientific papers
Palladium-Catalyzed Directed meta-Selective C?H Allylation of Arenes: Unactivated Internal Olefins as Allyl Surrogates
Achar, Tapas Kumar,Zhang, Xinglong,Mondal, Rahul,Shanavas,Maiti, Siddhartha,Maity, Sabyasachi,Pal, Nityananda,Paton, Robert S.,Maiti, Debabrata
supporting information, p. 10353 - 10360 (2019/07/04)
Palladium(II)-catalyzed meta-selective C?H allylation of arenes has been developed utilizing synthetically inert unactivated acyclic internal olefins as allylic surrogates. The strong σ-donating and π-accepting ability of pyrimidine-based directing group facilitates the olefin insertion by overcoming inertness of the typical unactivated internal olefins. Exclusive allyl over styrenyl product selectivity as well as E stereoselectivity were achieved with broad substrate scope, wide functional-group tolerance, and good to excellent yields. Late-stage functionalisations of pharmaceuticals were demonstrated. Experimental and computational studies shed light on the mechanism and point to key steric control in the palladacycle, thus determining product selectivities.
