64199-61-7 Usage
Uses
Used in Pharmaceutical Industry:
1-OLEOYL-2-PALMITOYL-SN-GLYCEROL is used as a pharmaceutical agent for its potential therapeutic properties. It can be utilized in the development of drugs targeting specific health conditions due to its unique structure and bioactivity.
Used in Cosmetic Industry:
In the cosmetic industry, 1-OLEOYL-2-PALMITOYL-SN-GLYCEROL is used as an ingredient in various skincare and beauty products. Its emollient and moisturizing properties make it suitable for improving skin hydration and texture.
Used in Food Industry:
1-OLEOYL-2-PALMITOYL-SN-GLYCEROL is used in the food industry as an emulsifier and stabilizer. Its ability to mix oil and water helps in creating stable food products with improved texture and shelf life.
Used in Research Applications:
In research settings, 1-OLEOYL-2-PALMITOYL-SN-GLYCEROL is used as a model compound to study lipid metabolism, membrane structure, and other biological processes. Its unique structure allows researchers to gain insights into the function and behavior of lipids in living organisms.
Check Digit Verification of cas no
The CAS Registry Mumber 64199-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,9 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64199-61:
(7*6)+(6*4)+(5*1)+(4*9)+(3*9)+(2*6)+(1*1)=147
147 % 10 = 7
So 64199-61-7 is a valid CAS Registry Number.
64199-61-7Relevant academic research and scientific papers
Du, Wenjun,Kulkarni, Suvarn S.,Gervay-Hague, Jacquelyn
, p. 2336 - 2338 (2007)
Per-O-silylated galactosyl iodides undergo α-glycosidation with fully functionalized glycolipids producing biologically relevant conjugates. The Royal Society of Chemistry.
ONE-POT SYNTHESIS OF ALPHA/BETA-O-GLYCOLIPIDS
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Page/Page column 20-21, (2008/12/04)
The present invention provides a one-pot method of preparing an unprotected α-O-glycolipid. The first step involves contacting a protected α-iodo sugar with a catalyst and a lipid comprising a hydroxy group, under conditions sufficient to prepare a protected α- O-glycolipid. The second step involves deprotecting the protected α-O-glycolipid under conditions sufficient to prepare the unprotected α-O-glycolipid, wherein the contacting and deprotecting steps are performed in a single vessel. The present invention also provides a one-pot method of preparing an unprotected β-O-glycolipid following the steps for the preparation of the unprotected α-O-glycolipid.
