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Diethyl piperazine-1,4-dicarboxylate is a chemical compound with the molecular formula C10H18N2O4. It is a versatile intermediate in the synthesis of pharmaceuticals, particularly for the production of antihistamines and antipsychotic drugs. diethyl piperazine-1,4-dicarboxylate has been found to possess potential therapeutic effects, such as antitumor and antiviral activities. Additionally, it serves as a corrosion inhibitor in metalworking fluids and as a stabilizer in PVC resin. Diethyl piperazine-1,4-dicarboxylate is considered to have low toxicity and is not classified as a hazardous substance by regulatory agencies.

5470-28-0

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5470-28-0 Usage

Uses

Used in Pharmaceutical Industry:
Diethyl piperazine-1,4-dicarboxylate is used as an intermediate in the synthesis of various pharmaceuticals, including antihistamines and antipsychotic drugs, due to its versatile chemical properties and potential therapeutic effects.
Used in Metalworking Fluids:
Diethyl piperazine-1,4-dicarboxylate is used as a corrosion inhibitor in metalworking fluids, helping to prevent the degradation of metal surfaces during manufacturing processes.
Used in PVC Resin:
Diethyl piperazine-1,4-dicarboxylate is used as a stabilizer in PVC resin, contributing to the material's durability and resistance to degradation.

Check Digit Verification of cas no

The CAS Registry Mumber 5470-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5470-28:
(6*5)+(5*4)+(4*7)+(3*0)+(2*2)+(1*8)=90
90 % 10 = 0
So 5470-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18N2O4/c1-3-15-9(13)11-5-7-12(8-6-11)10(14)16-4-2/h3-8H2,1-2H3

5470-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl piperazine-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names Piperazin-1,4-dicarbonsaeure-diaethylester

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:5470-28-0 SDS

5470-28-0Downstream Products

5470-28-0Relevant academic research and scientific papers

Novel piperazine based compounds as potential inhibitors for SARS-CoV-2 Protease Enzyme: Synthesis and molecular docking study

El-atawy, Mohamed,El-sadany, Samer K.,Hamed, Ezzat A.,Mosa, Tawfik M.,Omar, Alaa Z.

, (2021)

Structurally diverse piperazine-based compounds hybrid with thiadiazole, isatin or with sulfur/nitrogen, functionalities were synthesized. The structures of the new compounds were established based on their spectral data and elemental analysis. The physicochemical, bioactivity scores and pharmacokinetic behavior of all the prepared ligands were evaluated using in silico computational tools. The new piperazine ligands have been screened for their inhibition activity against SARS-CoV-2 protease enzyme using molecular docking analysis. The docking studies showed that all the ligands have been docked with negative dock energy onto the target protease protein. Moreover, Molecular interaction studies revealed that SARS-CoV-2 protease enzyme had strong hydrogen bonding interactions with piperazine ligands. The present in silico study thus, provided some guidance to facilitate drug design targeting the SARS-CoV-2 main protease.

Carbamate Synthesis Using a Shelf-Stable and Renewable C1 Reactant

Dobi, Zoltán,Reddy, B. Narendraprasad,Renders, Evelien,Van Raemdonck, Laurent,Mensch, Carl,De Smet, Gilles,Chen, Chen,Bheeter, Charles,Sergeyev, Sergey,Herrebout, Wouter A.,Maes, Bert U. W.

, p. 3103 - 3114 (2019/06/24)

4-Propylcatechol carbonate is a shelf-stable, renewable C1 reactant. It is easily prepared from renewable 4-propylcatechol (derived from wood) and dimethyl carbonate (derived from CO2) using a reactive distillation system. In this work, the 4-propylcatechol carbonate is used for the two-step synthesis of carbamates under mild reaction conditions. In the first step, 4-propylcatechol carbonate is treated with an alcohol at 50–80 °C in the presence of a Lewis acid catalyst, such as Zn(OAc)2?2 H2O. With liquid alcohols, no solvent is used and with solid alcohols 2-methyltetrahydrofuran is used as solvent. In the second step, the alkyl 2-hydroxy-propylphenyl carbonate intermediates obtained react with amines at room temperature in 2-methyltetrahydrofuran, forming the target carbamates and the byproduct 4-propylcatechol, which can be recycled into a carbonate reactant.

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