16892-10-7 Usage
Uses
Used in Water Treatment and Metal Cleaning Industry:
Phosphonic acid, bis(2-hydroxyethyl) ester is used as a chelating agent for binding metal ions, which helps in inhibiting the formation of scale and corrosion in water treatment and metal cleaning processes.
Used in Pharmaceutical Industry:
Phosphonic acid, bis(2-hydroxyethyl) ester is used as a pharmaceutical ingredient for treating conditions such as osteoporosis and Paget's disease. It functions by slowing down the breakdown of bone and reducing bone resorption, thereby improving bone health.
Used in Personal Care Products:
Phosphonic acid, bis(2-hydroxyethyl) ester is used in the formulation of personal care products, contributing to their effectiveness and performance.
Used in Chemical Synthesis:
Phosphonic acid, bis(2-hydroxyethyl) ester is utilized as a catalyst in chemical synthesis, enhancing the efficiency and selectivity of various chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 16892-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,9 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16892-10:
(7*1)+(6*6)+(5*8)+(4*9)+(3*2)+(2*1)+(1*0)=127
127 % 10 = 7
So 16892-10-7 is a valid CAS Registry Number.
16892-10-7Relevant academic research and scientific papers
H-tetraoxaspirophosphoranes as possible intermediates in the phosphonylation by phosphorous acid / oxiranes
Tzokov, Svetomir B.,Vassilev, Nikolay G.,Momtcheva, Rositza T.,Kaneti, Jose,Petkov, Dimiter D.
, p. 187 - 196 (2007/10/03)
The detailed 31P-NMR study of the mechanism of the ribozymomimetic phosphonylation with phosphorous acid / oxirane revealed consecutive formation of β-hydroxy H-phosphonate monoester, di-(β-hydroxyalkyl) H-phosphonate, alkylene H-phosphonate, β-hydroxyalkyl alkylene phosphite and the corresponding stereoelectronically stabilized pentacoordinated H-tetraoxaspirophosphorane. The equilibrium between the triphosphite and the spirophosphorane shifts towards the β-hydroxyalkyl alkylene phosphite at high temperatures. In the presence of alcohol and controlled amounts of water transesterification of the β-hydroxyalkyl alkylene phosphite to the corresponding alkyl alkylene phosphite, and hydrolysis to β-hydroxyalkyl alkyl H-phosphonate proceed at the elevated temperature. β-Hydroxyalkyl alkyl H-phosphonates are model compounds of the phosphodiester bond and undergo hydrolysis with a diol leaving in the presence of one equivalent of water.
