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DIETHYL (CARBOXYMETHYLAMINO)METHYLENEMALONATE is a versatile chemical compound that serves as a reagent in organic synthesis. It is a diethyl ester of carboxymethylaminomethylenemalonic acid, characterized by its ability to participate in a wide range of chemical reactions. DIETHYL (CARBOXYMETHYLAMINO)METHYLENEMALONATE is recognized for its structural versatility and diverse reactivity, which makes it a valuable building block in the synthesis of complex organic molecules. Its potential applications extend to the pharmaceutical and agrochemical industries, where it can be utilized to create various pharmacological and biologically active compounds.

54132-81-9

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54132-81-9 Usage

Uses

Used in Organic Synthesis:
DIETHYL (CARBOXYMETHYLAMINO)METHYLENEMALONATE is used as a reagent in organic synthesis for its ability to undergo various chemical reactions, facilitating the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DIETHYL (CARBOXYMETHYLAMINO)METHYLENEMALONATE is used as a building block for the synthesis of pharmacological compounds due to its structural versatility and potential to form biologically active molecules.
Used in Agrochemical Industry:
DIETHYL (CARBOXYMETHYLAMINO)METHYLENEMALONATE is utilized in the agrochemical industry as a component in the development of agrochemicals, taking advantage of its diverse reactivity to produce compounds with specific biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 54132-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,3 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54132-81:
(7*5)+(6*4)+(5*1)+(4*3)+(3*2)+(2*8)+(1*1)=99
99 % 10 = 9
So 54132-81-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H12NO2/c1-3-5(6(8)9)7-4-2/h5H,3-4H2,1-2H3,(H,8,9)

54132-81-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(3-ethoxy-2-ethoxycarbonyl-3-oxoprop-1-enyl)amino]acetic acid

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 -
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More Details:54132-81-9 SDS

54132-81-9Relevant academic research and scientific papers

Simultaneous HPLC analysis of biogenic amines, amino acids, and ammonium ion as aminoenone derivatives in wine and beer samples

Gomez-Alonso, Sergio,Hermosin-Gutierrez, Isidro,Garcia-Romero, Esteban

experimental part, p. 608 - 613 (2009/10/01)

A method has been developed for the simultaneous analysis of biogenic amines, amino acids, and the ammonium ion in wine and beer. Aminoenones formed by the reaction of amino acids, biogenic amines, and the ammonium ion with the derivatization reagent diet

A facile route to pyrroles, isoindoles and hetero fused analogues

Gabbutt, Christopher D.,Hepworth, John D.,Heron, B. Mark,Pugh, Samantha L.

, p. 2799 - 2808 (2007/10/03)

The decarboxylative cyclisation process where enamino acids derived from 1, 2-dimethylaminomethylene or 1, 2 hydroxymethylene-carbonyl compounds and amino acids gets converted into pyrroles, isoindoles and other fused pyrroles, was discussed. The cyclisat

An unusual ring expansion from the Zav'yalov pyrrole synthesis: Formation of oxacino[2,3-c]pyrroles

Gabbutt, Christopher D.,Hepworth, John D.,Heron, B. Mark,Elsegood, Mark R. J.,Clegg, William

, p. 289 - 290 (2007/10/03)

Enamino acids 2 and 5 undergo a facile cyclisation to afford the pyrrole 3 and isoindole 6 ring systems; a novel two atom ring expansion ensues when derivatives 5b,d are subjected to the cyclisation conditions, resulting in the formation of the new oxacin

Esterification of Amino Acids as Their 2,2-Bis(ethoxycarbonyl)vinyl Derivatives

Alaiz, Manuel,Giron, Julio,Hidalgo, Francisco Javier,Maza, Maria Pilar de la,Millan, Francisco,et al.

, p. 544 - 547 (2007/10/02)

A method to protect the amino group of the amino acids using diethyl (ethoxymethylene)malonate is described.The resulting derivatives are easily esterified with different alkylation agents.Elimination of the N-protecting group with bromine in chloroform a

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