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2-Propenoic acid, 2-methyl-, (diethoxyphosphinyl)methyl ester, also known as 2-Methylacrylic acid (diethoxyphosphinyl)methyl ester, is a chemical compound with the molecular formula C9H17O5P. It belongs to the class of organophosphorus compounds, specifically phosphinic esters. It is an ester of 2-methyl-2-propenoic acid and can be derived from a series of chemical reactions involving esterification and phosphonylation. Its attributes include a characteristic ester-like smell and unstable nature under certain conditions.

60161-88-8

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60161-88-8 Usage

Uses

Used in Chemical Synthesis:
2-Propenoic acid, 2-methyl-, (diethoxyphosphinyl)methyl ester is used as a chemical intermediate for the synthesis of various organic compounds. Its reactivity and phosphinic ester group make it a valuable building block in the preparation of complex molecules.
Used in Pharmaceutical Industry:
2-Propenoic acid, 2-methyl-, (diethoxyphosphinyl)methyl ester is used as a precursor in the development of pharmaceutical compounds. Its unique structure and reactivity can be exploited to create new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
2-Propenoic acid, 2-methyl-, (diethoxyphosphinyl)methyl ester is used as a starting material in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties allow for the creation of effective compounds that can protect crops from pests and diseases.
Used in Material Science:
2-Propenoic acid, 2-methyl-, (diethoxyphosphinyl)methyl ester is used as a component in the development of new materials, such as polymers and coatings. Its versatility in chemical reactions enables the creation of materials with specific properties, such as improved durability or resistance to environmental factors.

Check Digit Verification of cas no

The CAS Registry Mumber 60161-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,6 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60161-88:
(7*6)+(6*0)+(5*1)+(4*6)+(3*1)+(2*8)+(1*8)=98
98 % 10 = 8
So 60161-88-8 is a valid CAS Registry Number.

60161-88-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethoxyphosphorylmethyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names Diethylphosphonomethyl-methacrylat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:60161-88-8 SDS

60161-88-8Downstream Products

60161-88-8Relevant academic research and scientific papers

Rational Design of Polymers for Selective CO2 Reduction Catalysis

Leung, Jane J.,Vigil, Julian A.,Warnan, Julien,Edwardes Moore, Esther,Reisner, Erwin

supporting information, p. 7697 - 7701 (2019/05/15)

A series of copolymers comprising a terpyridine ligand and various functional groups were synthesized toward integrating a Co-based molecular CO2 reduction catalyst. Using porous metal oxide electrodes designed to host macromolecules, the Co-coordinated polymers were readily immobilized via phosphonate anchoring groups. Within the polymeric matrix, the outer coordination sphere of the Co terpyridine catalyst was engineered using hydrophobic functional moieties to improve CO2 reduction selectivity in the presence of water. Electrochemical and photoelectrochemical CO2 reduction were demonstrated with the polymer-immobilized hybrid cathodes, with a CO:H2 product ratio of up to 6:1 compared to 2:1 for a corresponding “monomeric” Co terpyridine catalyst. This versatile platform of polymer design demonstrates promise in controlling the outer-sphere environment of synthetic molecular catalysts, analogous to CO2 reductases.

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