56827-92-0 Usage
Description
Phosphoric acid, hexadecyl diphenyl ester, also known as Hexadecyl Diphenyl Phosphate, is a chemical compound with the molecular formula C33H57O4P. It is an organophosphate ester derived from phosphoric acid and has a variety of applications in different industries.
Uses
Used in Pharmaceutical Industry:
Phosphoric acid, hexadecyl diphenyl ester is used as a synthetic intermediate for the preparation of synthetic analogues of Irlbacholine. Irlbacholine is a novel antifungal plant metabolite isolated from Irlbachia Alata, which has potential applications in the development of new antifungal drugs.
Used in Chemical Research:
Phosphoric acid, hexadecyl diphenyl ester can be utilized as a research compound in the field of organic chemistry, particularly in the synthesis of various organophosphate esters and their derivatives. Its unique structure and properties make it a valuable compound for studying the reactivity and behavior of organophosphates in chemical reactions.
Used in Industrial Applications:
In the industrial sector, Phosphoric acid, hexadecyl diphenyl ester may find use as an additive or component in the formulation of various products, such as lubricants, plastics, and coatings. Its specific application would depend on the requirements of the product and the desired properties it can impart.
Check Digit Verification of cas no
The CAS Registry Mumber 56827-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,2 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56827-92:
(7*5)+(6*6)+(5*8)+(4*2)+(3*7)+(2*9)+(1*2)=160
160 % 10 = 0
So 56827-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C28H43O4P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-21-26-30-33(29,31-27-22-17-15-18-23-27)32-28-24-19-16-20-25-28/h15-20,22-25H,2-14,21,26H2,1H3
56827-92-0Relevant articles and documents
Inhibition of human erythrocyte membrane phosphatidylinositol 4-kinase by phospholipid analogues
Young,Downes,Jones,Milliner,Rana,Ward
, p. 537 - 549 (2007/10/02)
Analogues of phosphatidylinositol (PtdIns, 1) have been synthesized to investigate the structural requirements for inhibition of a PtdIns 4-kinase obtained from human erythrocyte membranes. While the presence of either D-1 or D-3 stereochemistry in the inositol moiety greatly influences the degree of inhibition produced by PtdIns analogues, the stereochemistry of the glycerol moiety is of little consequence. Neither structural feature however, makes a significant contribution to binding affinity. Competitive inhibitory activity was found to be retained (or even enhanced) in substantially simpler analogues consisting of 1 or 2 hydrocarbon chains attached to a charged phosphate head group, such as in the phosphatidic acids, 24 and 26. The observation that the phosphatidylinositol 4-phosphate (PtdIns 4P) and phosphatidic acid analogues (eg, 16 or 17, and 26 respectively) inhibit PtdIns 4-kinase may suggest that such species have a regulatory role in PtdIns turnover.
