51868-96-3 Usage
Uses
Used in Pharmaceutical Industry:
1-Pyrrolidinemethylphosphonic acid diethyl ester is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Pyrrolidinemethylphosphonic acid diethyl ester is utilized as an intermediate in the production of agrochemicals, aiding in the creation of pesticides and other agricultural products to enhance crop protection and yield.
Used as a Chelating Agent:
1-Pyrrolidinemethylphosphonic acid diethyl ester is employed as a chelating agent in chemical processes, where it helps to bind and stabilize metal ions, facilitating reactions and improving process efficiency.
Used as a Complexing Agent:
1-PYRROLIDINEMETHYLPHOSPHONIC ACID DIETHYL ESTER also serves as a complexing agent, enabling the formation of complexes with various molecules, which can be crucial in numerous chemical applications, including the synthesis of advanced materials and catalysts.
Check Digit Verification of cas no
The CAS Registry Mumber 51868-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,6 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51868-96:
(7*5)+(6*1)+(5*8)+(4*6)+(3*8)+(2*9)+(1*6)=153
153 % 10 = 3
So 51868-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H20NO3P/c1-3-12-14(11,13-4-2)9-10-7-5-6-8-10/h3-9H2,1-2H3/p+1
51868-96-3Relevant academic research and scientific papers
Efficient synthesis of phosphono- and phosphinoxidomethylated N-heterocycles under solvent-free microwave conditions
Prauda, Ibolya,Greiner, Istvan,Ludanyi, Krisztina,Keglevich, Gyoergy
, p. 317 - 322 (2007/10/03)
Simple N-heterocycles were converted to N-phosphono- and phosphinoxidomethyl derivatives by a solvent-free microwave-assisted condensation of the heterocycle, paraformaldehyde, and diethylphosphite or diphenylphosphine oxide in a convenient and, in most cases, efficient way. In contrast to an earlier report, imidazole proved to be unreactive in this type of phospha-Mannich reaction. Copyright Taylor & Francis Group, LLC.
Participation of Phosphonate Neighbour Groups with Dehydrogenations of Amines
Moehrle, Hans,Vetter, Wolfgang
, p. 1662 - 1671 (2007/10/02)
Aminophosphonates 1-5 are dehydrogenated with mercury EDTA to the corresponding lactams 6-9 and suprisingly to the formamide derivative 10.The different rate of ester hydrolysis of these acylamine compounds, the steric requirements and the reaction mechanisms are discussed. - Keywords: Aminomethanephosphonate, Mercury EDTA Dehydrogenation, Lactam, Formamide, Aminoalkylation
