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Dimethyl-5-mehtoxycarbonyl-2-oxopentyl phosphonate, 98%, is a high purity phosphonate ester compound characterized by the presence of two methyl groups, a carbonyl group, and a pentyl chain. It is renowned for its stability and reactivity, making it an essential building block in the synthesis of a variety of organic molecules, especially in the pharmaceutical and agrochemical sectors.

104227-38-5

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104227-38-5 Usage

Uses

Used in Pharmaceutical Industry:
Dimethyl-5-mehtoxycarbonyl-2-oxopentyl phosphonate, 98%, is utilized as a key intermediate in the synthesis of pharmaceutical compounds for its ability to contribute to the development of novel drugs with enhanced efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, Dimethyl-5-mehtoxycarbonyl-2-oxopentyl phosphonate, 98%, serves as a crucial component in the creation of innovative agrochemicals, including pesticides and herbicides, due to its role in enhancing the activity and selectivity of these products.
Used in Chemical Synthesis:
Dimethyl-5-mehtoxycarbonyl-2-oxopentyl phosphonate, 98%, is employed as a versatile building block in organic synthesis for its capacity to form a wide range of organic molecules with diverse applications across various industries, underpinned by its high purity and reliable performance.

Check Digit Verification of cas no

The CAS Registry Mumber 104227-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,2 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104227-38:
(8*1)+(7*0)+(6*4)+(5*2)+(4*2)+(3*7)+(2*3)+(1*8)=85
85 % 10 = 5
So 104227-38-5 is a valid CAS Registry Number.

104227-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 6-(dimethoxyphosphoryl)-5-oxohexanoate

1.2 Other means of identification

Product number -
Other names 5,7-Dimethyl-1,3-dihydro-imidazo[4,5-b]pyridin-2-on

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:104227-38-5 SDS

104227-38-5Relevant academic research and scientific papers

New Syntheses of Some Functionalized and Acetylenic β-Keto Phosphonates

Delamarche, Isabelle,Mosset, Paul

, p. 5453 - 5457 (1994)

β-Keto phosphonates ω-functionalized by an ester group 1a-f, by a hydroxyl 5, and with a triple bond conjugated to the carbonyl group 2a-c were prepared by reacting dimethyl (lithiomethyl)phosphonate (3) with adequate electrophiles.Cyclic anhydrides such as succinic and glutaric anhydrides were employed for the synthesis of the two first homologs 1a and 1b.To obtain the other longer homologs 1c-f, 3-acylthiazolidine-2-thiones 7a-d easily prepared using cheap 2-mercaptothiazoline proved to be the electrophiles of choice.On the other hand, the synthesis of keto phosphonates 2a-c required the use of N-methoxy-N-methylamides.

5-Oxo-ETE receptor antagonists

Gore, Vivek,Patel, Pranav,Chang, Chih-Tsung,Sivendran, Sashikala,Kang, Namin,Ouedraogo, Yannick P.,Gravel, Sylvie,Powell, William S.,Rokach, Joshua

, p. 3725 - 3732 (2013)

5-Oxo-ETE is the most powerful eosinophil chemoattractant among lipid mediators. Eosinophil infiltration into the lungs of asthmatics may be responsible for the late phase of inflammatory asthma. We have designed and synthesized a 5-oxo-ETE receptor antagonist, the purpose of which is to prevent eosinophil migration to the lung during an asthma attack and thereby reduce asthma symptoms.

Chemoselective synthesis of β-ketophosphonates using lithiated α-(trimethylsilyl)methylphosphonate

Specklin, Simon,Cossy, Janine

, p. 3302 - 3308 (2015/03/30)

A highly chemoselective synthesis of β-ketophosphonates from pentafluorophenyl esters and lithiated methyl α-(trimethylsilyl)methylphosphonate has been developed. This mild lithiated phosphonate reagent allows the synthesis of functionalized β-ketophosphonates in the presence of unactivated esters with high yields. This method has been compared with the standard lithiated methylphosphonate reagent.

Prostanoids: LXVI. A priori Postulated "9-LO Prostanoids"

Miftakhov,Imaeva,Fatykhov,Akhmetvaleev

, p. 47 - 54 (2007/10/03)

Based on the analysis of the literature data and the results given here, suggestions were made as to the pharmacological potential of "9-LO prostanoids." One representative of this class of compounds, (+)-2-decarboxy-2-ethyl-19,20-dinor-18-carboxyprostaglandin F2α, was synthesized starting from (-)-7α-hydroxy-6β-hydroxymethyl-cis-2-oxabicyclo[3.3.1]octan-3-one.

Total synthesis of a novel isoprostane IPF(2α)-I and its identification in biological fluids

Adiyaman, Mustafa,Lawson, John A.,Hwang, Seong-Woo,Khanapure, Subhash P.,FitzGerald, Garret A.,Rokach, Joshua

, p. 4849 - 4852 (2007/10/03)

The first tokai synthesis of IPF(2α)-I 25 is described using D-glucose as starting material. This novel isoprostane has been used to establish its presence in human urine.

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