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Phosphonic acid, [3-(3-methylphenyl)-2-oxopropyl]-, dimethyl ester is a versatile chemical compound derived from phosphonic acid, featuring a dimethyl ester functional group. Phosphonic acid, [3-(3-methylphenyl)-2-oxopropyl]-, dimethyl ester is highly soluble and stable in various solvents, making it suitable for a range of applications. Its unique structure allows it to effectively bind with metal ions, which is the basis for its use as a chelating agent and corrosion inhibitor in industrial settings.

61263-05-6

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61263-05-6 Usage

Uses

Used in Industrial Applications:
Phosphonic acid, [3-(3-methylphenyl)-2-oxopropyl]-, dimethyl ester is used as a chelating agent for its ability to bind with metal ions, preventing the formation of scale and corrosion in industrial equipment and pipelines. This helps maintain the efficiency and longevity of the equipment, reducing maintenance costs and downtime.
Used in Agricultural Products:
In the agricultural industry, Phosphonic acid, [3-(3-methylphenyl)-2-oxopropyl]-, dimethyl ester is used as a stabilizer and dispersing agent in the formulation of various products. Its chelating properties help to improve the solubility and distribution of active ingredients, ensuring even application and optimal performance of the products.
Overall, the dimethyl ester of phosphonic acid has a wide range of applications across different industries due to its chelating and inhibiting properties, contributing to improved performance, efficiency, and safety in various processes.

Check Digit Verification of cas no

The CAS Registry Mumber 61263-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,6 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61263-05:
(7*6)+(6*1)+(5*2)+(4*6)+(3*3)+(2*0)+(1*5)=96
96 % 10 = 6
So 61263-05-6 is a valid CAS Registry Number.

61263-05-6SDS

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 1-dimethoxyphosphoryl-3-(3-methylphenyl)propan-2-one

1.2 Other means of identification

Product number -
Other names -

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:61263-05-6 SDS

61263-05-6Downstream Products

61263-05-6Relevant academic research and scientific papers

A Convenient Procedure for the Synthesis of 2,2,2-Trifluoroethyl Methyl 2-Oxoalkylphosphonates

Molnár, Katalin,Behra, Julien,Takács, László,Kádár, Mihály,Kardos, Zsuzsanna,Faigl, Ferenc

supporting information, p. 677 - 680 (2015/07/20)

(Figure Presented) A convenient and versatile method was developed for the synthesis of 2,2,2-trifluoroethyl methyl 2-oxoalkylphosphonates starting from dimethyl phosphonates by alkaline hydrolysis followed by esterification with 2,2,2-trifluoroethanol using diisopropylcarbodiimide (DIC) in the presence of 4-(dimethylamino)pyridine (DMAP) catalyst following the Steglich protocol.

Discovery of a novel EP2/EP4 dual agonist with high subtype-selectivity

Kambe, Tohru,Maruyama, Toru,Nakano, Masayuki,Nakai, Yoshihiko,Yoshida, Tadahiro,Matsunaga, Naoki,Oida, Hiroji,Konaka, Akira,Maruyama, Takayuki,Nakai, Hisao,Toda, Masaaki

scheme or table, p. 396 - 401 (2012/02/16)

A series of γ-lactam prostaglandin E1 analogs bearing a 16-phenyl moiety in the ω-chain and aryl moiety in the α-chain were synthesized and biologically evaluated. Among the tested compounds, γ-lactam PGE analog 3 designed as a structural hybrid of 1 and 2 was discovered as the most optimized EP2/EP4 dual agonist with excellent subtype-selectivity (Ki values: mEP2 = 9.3 nM, mEP4 = 0.41 nM). A structure-activity relationship study is presented.

Discovery of orally available 8-aza-5-thiaProstaglandin E1 analogs as highly selective EP4 agonists

Kambe, Tohru,Maruyama, Toru,Nakano, Masayuki,Yamaura, Yoshiyuki,Shono, Tomoyuki,Seki, Akiteru,Sakata, Kiyoto,Maruyama, Takayuki,Nakai, Hisao,Toda, Masaaki

, p. 1523 - 1534 (2012/01/13)

Analogs 8-aza-16-aryl prostaglandin E1 (PGE1) and 8-aza-5-thia-16-arylPGE1 were synthesized and evaluated with respect to their subtype receptor affinity and EP4 agonist activity for the purposes of identifying sub-type- selective EP

(15R)-16-m-Tolyl-17,18,19,20-tetranorisocarbacyclin: ein stabiler, hochselekiver Ligand mit hoher Bindungsaffinitaet fuer einen Prostacyclin-Rezeptor im zentralen Nervensystem

Suzuki, Masaaki,Kato, Koichi,Noyori, Ryoji,Watanabe, Yumiko,Takechi, Hajime,et al.

, p. 366 - 369 (2007/10/03)

Keywords: Prostacyclinrezeptoren; Molekulare Sonden; Tolylisocarbacyclin

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