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[2-(2-Chloro-ethoxy)-ethyl]-phosphonic acid, also known as 2-(2-chloroethoxy)ethylphosphonic acid, is a technical-grade chemical compound with a unique structure that features a phosphonic acid group attached to a 2-chloroethoxyethyl moiety. [2-(2-Chloro-ethoxy)-ethyl]-phosphonic acid exhibits interesting chemical properties and potential applications in various fields.

69404-51-9

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69404-51-9 Usage

Uses

Used in Biological Studies:
[2-(2-Chloro-ethoxy)-ethyl]-phosphonic acid is used as a research chemical for studying the composition and properties of technical ethephon. It aids in understanding the behavior of [2-(2-Chloro-ethoxy)-ethyl]-phosphonic acid in biological systems and its potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [2-(2-chloroethoxy)ethylphosphonic acid] is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
[2-(2-Chloro-ethoxy)-ethyl]-phosphonic acid is also used in chemical research as a reagent or catalyst in various chemical reactions. Its ability to form stable complexes with metal ions and its reactivity make it a valuable tool in the synthesis of new chemical compounds and materials.
Used in Environmental Applications:
In environmental applications, [2-(2-chloroethoxy)ethylphosphonic acid] can be used as a component in the development of new technologies for water and soil treatment. Its ability to form stable complexes with metal ions and its potential to interact with organic pollutants make it a promising candidate for environmental remediation efforts.
Overall, [2-(2-chloroethoxy)ethylphosphonic acid] is a versatile compound with a wide range of potential applications in various industries, including pharmaceuticals, chemical research, and environmental applications. Its unique structure and properties make it an interesting subject for further study and development.

Check Digit Verification of cas no

The CAS Registry Mumber 69404-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,0 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69404-51:
(7*6)+(6*9)+(5*4)+(4*0)+(3*4)+(2*5)+(1*1)=139
139 % 10 = 9
So 69404-51-9 is a valid CAS Registry Number.

69404-51-9Downstream Products

69404-51-9Relevant academic research and scientific papers

Synthesis and antiviral activities of hexadecyloxypropyl prodrugs of acyclic nucleoside phosphonates containing guanine or hypoxanthine and a (S)-HPMP or PEE acyclic moiety

Tichy, Tomas,Dracinsky, Martin,Krecmerova, Marcela,Andrei, Graciela,Snoeck, Robert,Balzarini, Jan

, p. 307 - 314,8 (2020/07/31)

Hexadecyloxypropyl esters of acyclic nucleoside phosphonates containing guanine (G) or hypoxanthine (Hx) and a (S)-[3-hydroxy-2-(phosphonomethoxy) propyl] [(S)-HPMP] or 2-(2-phosphonoethoxy)ethyl (PEE) acyclic moiety have been prepared. The activity of the prodrugs was evaluated in vitro against different virus families. Whereas ester derivatives of PEEHx and (S)-HPMPHx were antivirally inactive, monoesters of PEEG, and mono- and diesters of (S)-HPMPG showed pronounced antiviral activity against vaccinia virus and/or herpesviruses. Monoesters of (S)-HPMPG emerged as the most potent and selective derivatives against these DNA viruses. None of the compounds were inhibitory against RNA viruses and retroviruses. Crown Copyright

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