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Triethyl 4-oxopyrrolidine-1,2,3-tricarboxylate is a complex organic compound characterized by a molecular formula of C14H19NO9. It features a pyrrolidine ring with a carbonyl group at the fourth position, flanked by three carboxyl groups at positions one, two, and three. This tricarboxylic acid ester is recognized for its role as a building block in the synthesis of various compounds and holds potential in pharmaceuticals and drug discovery due to its distinctive structure and reactivity. However, it is imperative to exercise caution during its handling, given the inherent hazards and risks associated with its use.

41263-63-2

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41263-63-2 Usage

Uses

Used in Pharmaceutical and Drug Discovery:
Triethyl 4-oxopyrrolidine-1,2,3-tricarboxylate serves as a key intermediate in the synthesis of pharmaceutical compounds, leveraging its unique structure and reactivity for the development of new drugs.
Used in Industrial Chemical Synthesis:
As a building block, triethyl 4-oxopyrrolidine-1,2,3-tricarboxylate is utilized in the creation of a variety of chemical compounds, contributing to the advancement of industrial processes and the production of novel materials.

Check Digit Verification of cas no

The CAS Registry Mumber 41263-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41263-63:
(7*4)+(6*1)+(5*2)+(4*6)+(3*3)+(2*6)+(1*3)=92
92 % 10 = 2
So 41263-63-2 is a valid CAS Registry Number.

41263-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl 4-oxopyrrolidine-1,2,3-tricarboxylate

1.2 Other means of identification

Product number -
Other names 4-oxo-pyrrolidine-1,2,3-tricarboxylic acid triethyl ester

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:41263-63-2 SDS

41263-63-2Downstream Products

41263-63-2Relevant academic research and scientific papers

Synthesis and stereochemistry of some 1,2,3,4-tetrasubstituted pyrrolidines

Rozing, G. P.,Koning, H. de,Huisman, H. O.

, p. 359 - 368 (2007/10/02)

Several isomeric 1,2,3-trisubstituted 4-hydroxypyrrolidines were obtained from reductions of 1,3-(diethoxycarbonyl)-2-methyl-4-oxopyrrolidine and 1,2-(diethoxycarbonyl)-3-methyl-4-oxopyrrolidine.The chemistry of these reductions is discussed.The relative configurations of the hydroxypyrrolidines were determined by chemical interconversions and spectroscopic methods, providing 1H NMR and 13C NMR data which are useful in structural assignment of other pyrrolidine derivatives.

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