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54132-81-9

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54132-81-9 Usage

General Description

DIETHYL (CARBOXYMETHYLAMINO)METHYLENEMALONATE is a chemical compound that is commonly used as a reagent in organic synthesis. It is a diethyl ester of carboxymethylaminomethylenemalonic acid and is often utilized in the preparation of various pharmacological and biologically active compounds. DIETHYL (CARBOXYMETHYLAMINO)METHYLENEMALONATE is known for its ability to undergo a variety of chemical reactions, making it a versatile building block in the synthesis of complex organic molecules. Additionally, it has potential applications in the pharmaceutical and agrochemical industries due to its diverse reactivity and structural versatility.

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54132-81-9 SDS

54132-81-9Relevant articles and documents

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

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

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