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Ethylphosphonic acid, dipropyl ester, also known as dipropyl ethylphosphonate, is an organophosphorus compound with the chemical formula C7H15O3P. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 178.17 g/mol. Ethylphosphonic acid, dipropyl ester is primarily used as a precursor in the synthesis of various organophosphorus compounds, such as pesticides and flame retardants. It is also employed as a reagent in the preparation of other phosphonic acid derivatives. Due to its potential toxicity and environmental impact, handling and disposal of this chemical should be done with caution, following proper safety protocols and regulations.

6163-76-4

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6163-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6163-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,6 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6163-76:
(6*6)+(5*1)+(4*6)+(3*3)+(2*7)+(1*6)=94
94 % 10 = 4
So 6163-76-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H18N2O2/c1-26-18-11-7-10-17(15-18)24-21(14-16-8-3-2-4-9-16)23-20-13-6-5-12-19(20)22(24)25/h2-13,15H,14H2,1H3

6163-76-4Downstream Products

6163-76-4Relevant academic research and scientific papers

Microwave-assisted ionic liquid-catalyzed selective monoesterification of alkylphosphonic acids—an experimental and a theoretical study

Harsági, Nikoletta,Henyecz, Réka,ábrányi-Balogh, Péter,Drahos, László,Keglevich, Gy?rgy

, (2021/09/07)

It is well-known that the P-acids including phosphonic acids resist undergoing direct es-terification. However, it was found that a series of alkylphoshonic acids could be involved in mo-noesterification with C2–C4 alcohols under microwave (MW) irradiation in the presence of [bmim][BF4] as an additive. The selectivity amounted to 80–98%, while the isolated yields fell in the range of 61–79%. The method developed is a green method for P-acid esterification. DFT calculations at the M062X/6–311+G (d,p) level of theory (performed considering the solvent effect of the corresponding alcohol) explored the three-step mechanism, and justified a higher enthalpy of activation (160.6–194.1 kJ·mol–1) that may be overcome only by MW irradiation. The major role of the [bmim][BF4] additive is to increase the absorption of MW energy. The specific chemical role of the [BF4] anion of the ionic liquid in an alternative mechanism was also raised by the computations.

P-Toluenesulfonic acid-Celite as a reagent for synthesis of esters of alkylphosphonic acids under solvent-free conditions

Gupta, Arvind K.,Kumar, Rajesh,Dubey, Devendra K.,Kaushik

, p. 328 - 331 (2008/02/10)

The coupling reaction of alkylphosphonic acids and alcohols on the surface of p-toluenesulfonic acid-Celite under mild and solvent-free conditions gave the corresponding phosphonates in excellent yields. This method provides a useful rapid synthesis of phosphonates for use in the unambiguous identification of chemical warfare agents.

An efficient method for the esterification of phosphonic and phosphoric acids using silica chloride

Sathe, Manisha,Gupta, Arvind K.,Kaushik

, p. 3107 - 3109 (2007/10/03)

Silica chloride is used as an effective heterogeneous catalyst for the rapid esterification of alkyl/aryl phosphonic/phosphoric acids to their corresponding alkyl/aryl phosphonates/phosphates under mild conditions with quantitative yields.

Surface-mediated solid phase reactions: A simple, efficient and base-free synthesis of phosphonates and phosphates on Al2O3

Acharya, Jyotiranjan,Shakya, Purushottam D.,Pardasani, Deepak,Palit, Meehir,Dubey, Devendra K.,Gupta, Arvind K.

, p. 194 - 196 (2007/10/03)

Al2O3-supported solvent free condensation of alkylphosphonic dichlorides with alcohols at room temperature yielded phosphorus esters in excellent yields.

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