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Phosphonic acid, [amino(4-methoxyphenyl)methyl]-, diphenyl ester is a chemical compound that belongs to the class of phosphonic acids and related compounds. It is a diphenyl ester derivative of a phosphonic acid with the amino(4-methoxyphenyl)methyl group. This versatile chemical intermediate is characterized by its potential applications in the synthesis of a wide range of organic compounds, pharmaceuticals, agrochemicals, and materials.

127825-05-2

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127825-05-2 Usage

Uses

Used in Organic Synthesis:
Phosphonic acid, [amino(4-methoxyphenyl)methyl]-, diphenyl ester is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the formation of new chemical bonds and the creation of complex molecules, making it a valuable component in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Phosphonic acid, [amino(4-methoxyphenyl)methyl]-, diphenyl ester is used as a building block for the development of new drugs. Its ability to form stable bonds with other molecules makes it a promising candidate for the synthesis of pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
Phosphonic acid, [amino(4-methoxyphenyl)methyl]-, diphenyl ester is also utilized in the agrochemical industry for the synthesis of pesticides and other agricultural chemicals. Its versatility in forming stable chemical bonds allows for the development of effective and targeted agrochemicals.
Used in Material Science:
In the field of material science, Phosphonic acid, [amino(4-methoxyphenyl)methyl]-, diphenyl ester is used in the development of new materials with specific properties. Its ability to form stable bonds with other molecules contributes to the creation of materials with unique characteristics, such as improved strength, durability, or chemical resistance.
It is crucial to handle Phosphonic acid, [amino(4-methoxyphenyl)methyl]-, diphenyl ester with care and follow proper safety protocols to minimize potential health and environmental hazards associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 127825-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,8,2 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127825-05:
(8*1)+(7*2)+(6*7)+(5*8)+(4*2)+(3*5)+(2*0)+(1*5)=132
132 % 10 = 2
So 127825-05-2 is a valid CAS Registry Number.

127825-05-2SDS

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 diphenoxyphosphoryl-(4-methoxyphenyl)methanamine

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:127825-05-2 SDS

127825-05-2Relevant academic research and scientific papers

Synthesis of phosphonodipeptide conjugates of ursolic acid and their homologs

Deng, Sheng-Lou,Baglin, Isabelle,Nour, Mohammed,Cave, Christian

, p. 55 - 65 (2008/04/05)

To prepare novel derivatives of naturally bioactive 3β-hydroxy-urs-12- en-28-oic acid (ursolic acid) with unusual properties and broad spectrum of activities, a number of chemical reactions were conducted. First, a variety of a-aminophosphonates were prepared by a series of reactions involving the three-component Mannich type reaction as a key step. Second, an array of phosphonodipeptides and their homologs was synthesized through multistep reactions including condensation of phthalic anhydride with glycine or β-alanine, chlorination of N-blocked amino acids, coupling of acid chloride with α-aminophosphonates and sequential hydrazinolysis. Finally, new classes of phosphonodipeptide conjugates of ursolic acid and their homologs were obtained by condensation of 3β-acetoxy-urs-12-en-28-oyl chloride with phosphonodipeptides and their homologs.

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