19805-23-3 Usage
Description
()-3-[[(2-aminoethoxy)hydroxyphosphinoyl]oxy]-2-hydroxypropyl hexadecanoate is a phosphonate ester derivative of hexadecanoic acid, featuring a hydroxyphosphinoyloxy group attached to a 2-aminoethoxy substituted hydroxypropyl chain. This unique structure and properties make it a promising candidate for various applications in pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
()-3-[[(2-aminoethoxy)hydroxyphosphinoyl]oxy]-2-hydroxypropyl hexadecanoate is used as a potential drug delivery system for enhancing the bioavailability and therapeutic outcomes of various pharmaceutical agents.
Used in Agrochemical Industry:
()-3-[[(2-aminoethoxy)hydroxyphosphinoyl]oxy]-2-hydroxypropyl hexadecanoate is used as a potential surfactant, emulsifier, or stabilizer in agrochemical formulations to improve their performance and effectiveness.
Used in Materials Science:
()-3-[[(2-aminoethoxy)hydroxyphosphinoyl]oxy]-2-hydroxypropyl hexadecanoate is used as a potential corrosion inhibitor in materials science applications, providing protection against corrosion and extending the lifespan of materials.
Further research is required to fully understand the properties and potential applications of ()-3-[[(2-aminoethoxy)hydroxyphosphinoyl]oxy]-2-hydroxypropyl hexadecanoate, as its unique structure and properties may lead to additional uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19805-23-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,0 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19805-23:
(7*1)+(6*9)+(5*8)+(4*0)+(3*5)+(2*2)+(1*3)=123
123 % 10 = 3
So 19805-23-3 is a valid CAS Registry Number.
19805-23-3Relevant articles and documents
Rapid tin-mediated access to a lysophosphatidylethanolamine (LPE) library: Application to positional LC/MS analysis for hepatic LPEs in non-alcoholic steatohepatitis model mice
Furukawa, Takayuki,Fuda, Hirotoshi,Miyanaga, Satoshi,Watanabe, Chinatsu,Chiba, Hitoshi,Hui, Shu-Ping
, p. 133 - 138 (2016/10/11)
Even though lysophospholipids have attracted much interest in recent years on account of their unique bioactivity, research related to lysophospholipids is usually hampered by problems associated with standard sample preparation and discrimination of regioisomers. Herein, we demonstrate a quick tin-chemistry-based synthetic route to lysophosphatidylethanolamines (LPEs) and its application in the positional analysis of hepatic LPEs in non-alcoholic steatohepatitis (NASH) model mice. We found that the preference of hepatic LPE regioisomer largely depends on the unsaturation of acyl chain in both control and NASH model mice. In addition, hepatic C18:2-LPE and C20:5-LPE levels were significantly lower in the NASH model mice than those in the control. The LC/MS technique based on the library of LPE regioisomers allows an accurate observation of hepatic LPE metabolism and might provide useful information to elucidate yet ambiguous pathogenesis of NASH.
The synthesis of phospholipids. I. Phosphatidyl and lysophosphatidyl ethanolamines.
Billimoria,Lewis
, p. 1404 - 1412 (2007/10/12)
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