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1-Ethylphosphonic cyclic anhydride is a chemical compound characterized by the molecular formula C5H9O3P. It features a cyclic phosphonate anhydride structure with a five-membered ring and an ethyl group attached to the phosphorus atom. 1-Ethylphosphonic cyclic anhydride is recognized for its versatile reactivity and potential in a range of chemical applications, making it of interest to researchers and industry professionals.

145007-52-9

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145007-52-9 Usage

Uses

Used in Organic Synthesis:
1-Ethylphosphonic cyclic anhydride is utilized as a reagent in organic synthesis, particularly for the formation of phosphonate esters and amides. Its unique structure and reactivity make it a valuable component in creating a variety of chemical compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1-Ethylphosphonic cyclic anhydride is used as a key intermediate in the synthesis of various drugs. Its ability to form phosphonate esters and amides contributes to the development of new medicinal compounds with potential therapeutic applications.
Used in Agrochemical Production:
Similarly, in agrochemicals, 1-Ethylphosphonic cyclic anhydride serves as an essential building block for the creation of pesticides and other agricultural chemicals, enhancing crop protection and yield.
Used in Flame Retardant Development:
1-Ethylphosphonic cyclic anhydride has potential applications in the development of flame retardants, where its phosphorus content can enhance the fire-resistant properties of materials, contributing to improved safety standards in various industries.
Used in Advanced Polymer Materials:
As a building block for advanced polymer materials, 1-Ethylphosphonic cyclic anhydride contributes to the development of new polymers with specialized properties, such as enhanced thermal stability, flame resistance, or other desirable characteristics for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 145007-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 145007-52:
(8*1)+(7*4)+(6*5)+(5*0)+(4*0)+(3*7)+(2*5)+(1*2)=99
99 % 10 = 9
So 145007-52-9 is a valid CAS Registry Number.

145007-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-triethyl-1,3,5,2λ<sup>5</sup>,4λ<sup>5</sup>,6λ<sup>5</sup>-trioxatriphosphinane 2,4,6-trioxide

1.2 Other means of identification

Product number -
Other names 1,3,5,2,4,6-Trioxatriphosphorinane,2,4,6-triethyl-,2,4,6-trioxide

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:145007-52-9 SDS

145007-52-9Upstream product

145007-52-9Downstream Products

145007-52-9Relevant academic research and scientific papers

METHOD FOR THE PRODUCTION OF CYCLIC PHOSPHONIC ACID ANHYDRIDES

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Page/Page column 8; 9, (2008/06/13)

Disclosed is a method for producing cyclic phosphonic acid anhydrides of formula (III) by a) reacting phosphonic acid derivatives of formula (I) with acetic anhydride at a temperature ranging between 30 and 150 °C while separating a mixture of ethanoic acid and acetic anhydride by means of distillation, b) then reactively distilling the oligomeric phosphonic acid anhydrides of formula (II) obtained in step a) and transforming the same into the corresponding cyclic trimeric phosphonic acid anhydrides of formula (III), n representing a number between 0 and 300 while R represents allyl, aryl, or open-chain, cyclic, or branched C1 to C8 alkyl radicals, aryloxy, allyloxy, or alkoxy comprising open-chain, cyclic, or branched C1 to C8 alkyl radicals. Preferably, the cyclic trimeric phosphonic acid anhydrides formed in step b) are immediately dissolved in an organic solvent that exhibits an inert behavior relative thereto.

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