5835-62-1 Usage
Uses
Used in Industrial Applications:
Phosphonic acid, (2-phenoxyethyl)is used as a chelating agent for binding to metal ions, forming stable complexes. This property makes it valuable in various industrial processes where metal ion management is crucial.
Used in Environmental Applications:
As a corrosion inhibitor, phosphonic acid, (2-phenoxyethyl)is employed to prevent the degradation of metal surfaces, thus protecting them from environmental factors that could lead to corrosion.
Used in Pharmaceutical Synthesis:
Phosphonic acid, (2-phenoxyethyl)is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, phosphonic acid, (2-phenoxyethyl)serves as an important building block in the creation of agrochemicals, such as pesticides and herbicides, to improve agricultural productivity and crop protection.
Safety Precautions:
It is important to handle Phosphonic acid, (2-phenoxyethyl)with care, as it can be harmful if ingested, inhaled, or in contact with skin or eyes. Proper safety measures should be taken to minimize exposure and ensure safe handling during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5835-62-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5835-62:
(6*5)+(5*8)+(4*3)+(3*5)+(2*6)+(1*2)=111
111 % 10 = 1
So 5835-62-1 is a valid CAS Registry Number.
5835-62-1Relevant academic research and scientific papers
A nonhydrolyzable analogue of phosphotyrosine, and related aryloxymethano- and aryloxyethano-phosphonic acids as motifs for inhibition of phosphatases
Iyer, Subashree,Younker, Jarod M.,Czyryca, Przemyslaw G.,Hengge, Alvan C.
, p. 5931 - 5935 (2007/10/03)
Nonhydrolyzable analogues of both stereoisomers of phosphotyrosine, and a series of related aryloxy (or thio) methyl and aryloxy (or thio) ethyl phosphonic acids of the general formula RX-(CH2)n-PO 3H2 (where X = O or S and n = 1 or 2), have been tested as nonhydrolyzable mimetics of phosphatase substrates. These compounds were tested against a panel of phosphatases (two alkaline phosphatases, a protein-tyrosine phosphatase, and two serine/threonine phosphatases) with different active site motifs. The compounds exhibit competitive inhibition toward all enzymes tested, with the best inhibition expressed toward the Ser/Thr phosphatases. The stereoisomers of the phosphotyrosine analogues exhibited an unexpected difference in their inhibitory properties toward the protein-tyrosine phosphatase from Yersinia. The Ki for the d isomer is 33-fold lower than that of the l isomer, and is more than an order of magnitude lower than the reported Km of the substrate l-phosphotyrosine.
