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Ethyl 1-(3-ethoxy-3-oxopropyl)-5-oxoprolinate is a complex organic chemical compound with the molecular formula C11H16O6. It is a derivative of proline, an amino acid, and features a proline core with an ethyl ester group and a 3-ethoxy-3-oxopropyl side chain. ethyl 1-(3-ethoxy-3-oxopropyl)-5-oxoprolinate is characterized by its ability to form salts and is often used in the synthesis of various pharmaceuticals and biologically active molecules due to its unique structure and reactivity. It plays a significant role in the development of new drugs and can be found in research related to medicinal chemistry and chemical biology.

5447-61-0

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5447-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5447-61-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5447-61:
(6*5)+(5*4)+(4*4)+(3*7)+(2*6)+(1*1)=100
100 % 10 = 0
So 5447-61-0 is a valid CAS Registry Number.

5447-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-(3-ethoxy-3-oxopropyl)-5-oxopyrrolidine-2-carboxylate

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

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More Details:5447-61-0 SDS

5447-61-0Downstream Products

5447-61-0Relevant academic research and scientific papers

A general N-alkylation procedure for ethyl pyroglutamate

Simandan, Tiberiu,Smith, Michael B.

, p. 1827 - 1838 (2007/10/03)

Despite several reported procedures for coupling alkyl halides and 5-oxoproline esters (pyroglutamate derivatives), no general method has been described. The reaction of pyrroglutamate with sodium hydride, in anhydrous THF in the presence of the halide, p

Studies on pyrrolidinones. Michael reaction of glutamic acid and diethylglutamate

Rigo, Benoit,Couturier, Daniel,Kolocouris, Nicolas

, p. 1769 - 1772 (2007/10/02)

Starting from glutamic acid or diethyl glutamate, some derivatives of N-(2-carboxyethyl), N-(3-oxobutyl) and N-(2-cyanoethyl)pyroglutamic acid were synthesized.

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