864068-45-1 Usage
General Description
Phosphonic acid, P-[[[(4-Methylphenyl)sulfonyl]oxy]Methyl]-, Mono[3-(hexadecyloxy)propyl] ester is a chemical compound used primarily as a surfactant and dispersing agent in various products, including coatings, adhesives, and personal care items. It is characterized by a phosphonic acid group, a sulfonyl group, and a hexadecyloxypropyl group. The compound's structure and properties make it effective in promoting adhesion, reducing surface tension, and enhancing the compatibility of different ingredients in formulations. It is commonly used in the production of water-based paints, varnishes, and other coatings, where it improves the wetting and dispersing of pigments and fillers. Additionally, Phosphonic acid, P-[[[(4-Methylphenyl)sulfonyl]oxy]Methyl]-, Mono[3-(hexadecyloxy)propyl] ester is also utilized as a corrosion inhibitor in metalworking fluids and as an antiscalant in water treatment applications. Overall, this chemical compound plays a crucial role in improving the performance and properties of a wide range of industrial and consumer products.
Check Digit Verification of cas no
The CAS Registry Mumber 864068-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,0,6 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 864068-45:
(8*8)+(7*6)+(6*4)+(5*0)+(4*6)+(3*8)+(2*4)+(1*5)=191
191 % 10 = 1
So 864068-45-1 is a valid CAS Registry Number.
864068-45-1Relevant articles and documents
Phosphonate Ester Derivatives and Methods of Synthesis Thereof
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, (2012/03/26)
The disclosure describes methods of synthesis of phosphonate ester derivatives. Preferred methods according to the disclosure allow for large-scale preparation of phosphonate ester compounds having high purity. In some embodiments, preferred methods accor
METHODS FOR PREPARATION OF NUCLEOSIDE PHOSPHONATE ESTERS
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Page/Page column 30, (2010/02/14)
A process is provided for the preparation of lipophilic monoesters of formula (3) and their stereoisomers. The process includes the steps of esterification of a phosphonate with a lipophilic alcohol, then allowing the resultant product to react with a sui
