53892-41-4 Usage
Synonyms
C6PC
Type
Synthetic phospholipid derivative
Function
Surfactant and emulsifier
Applications
Pharmaceutical and cosmetic products
Structure
Hexanoyl (C6) fatty acid attached to the sn-2 position of the glycerol backbone and a phosphocholine head group
Ability
Disrupt lipid membranes and promote lipid bilayer fusion
Utility
Drug delivery systems, component in liposomes for drug and bioactive compound delivery
Surface activity
Used in formulations for emulsions, creams, and ointments
Additional uses
Medical devices and diagnostic reagents
Check Digit Verification of cas no
The CAS Registry Mumber 53892-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,9 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53892-41:
(7*5)+(6*3)+(5*8)+(4*9)+(3*2)+(2*4)+(1*1)=144
144 % 10 = 4
So 53892-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H40NO8P/c1-6-8-10-12-19(22)26-16-18(29-20(23)13-11-9-7-2)17-28-30(24,25)27-15-14-21(3,4)5/h18H,6-17H2,1-5H3
53892-41-4Relevant articles and documents
Selective Acylation of Nucleosides, Nucleotides, and Glycerol-3-phosphocholine in Water
Fernández-García, Christian,Powner, Matthew W.
supporting information, p. 78 - 83 (2016/12/26)
A convenient selective synthesis of 2′,3′-di-O-acetyl-nucleotide-5′-phosphates, 2′,3′-di-O-acetyl-nucleotide-5′-triphosphates and 2′,3′,5′-tri-O-acetyl-nucleosides in water has been developed. Furthermore, a long-chain selective glycerol-3-phosphocholine diacylation is elucidated. These reactions are environmentally benign, rapid, high yielding, and the products are readily purified. Importantly, this reaction may indicate a prebiotically plausible reaction pathway for the selective acylation of key metabolites to facilitate their incorporation into protometabolism.
