56968-65-1

Basic information

• Product Name: 1-Piperazinepropanoic acid, 4-phenyl-, ethyl ester
• CAS NO: 56968-65-1
• Molecular Formula: C15H22N2O2
• Molecular Weight: 262.352
• Mol File: 56968-65-1.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-Piperazinepropanoic acid, 4-phenyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperazinepropanoic acid, 4-phenyl-, ethyl ester(56968-65-1)
• EPA Substance Registry System: 1-Piperazinepropanoic acid, 4-phenyl-, ethyl ester(56968-65-1)

Safety Data

• Hazardous Substances Data: 56968-65-1(Hazardous Substances Data)

Usage

General Description

1-Piperazinepropanoic acid, 4-phenyl-, ethyl ester is a chemical compound that falls under the category of esters. It is formed by the reaction between 1-piperazinepropanoic acid, 4-phenyl- and ethyl alcohol. 1-Piperazinepropanoic acid, 4-phenyl-, ethyl ester is often used in the field of pharmaceuticals, where it can act as an intermediate for the synthesis of various drugs. It is also known for its potential biological activity and has been studied for its potential applications in the treatment of various diseases. However, it is important to handle this compound with caution, as it may pose certain health and safety risks if not used properly.

Upstream product

• 92-54-6 4-phenyl-1-piperazine 
• 539-74-2 Ethyl 3-bromopropionate 
• 140-88-5 ethyl acrylate 

Downstream Products

• 124078-87-1 3-(4-phenyl-1-piperazinyl)-propionic acid 
• 63853-93-0 sodium salt of 1-[2-(4-phenylpiperazinyl-1)-ethyl]-3-(2-hydroxy-6-methoxyphenyl)-propane-1,3-dione 
• 67514-07-2 1-phenyl-4-(3-hydroxypropyl)piperazine 

Relevant articles and documents

Green synthesis of Ag@Au bimetallic regenerated cellulose nanofibers for catalytic applications

The green synthesis of nanocomposites has attracted huge consideration in recent years due to its positive environmentally friendly impact. The present study reports the first bimetallic Ag-Au cellulose nanofiber composite (Ag@Au/CNCs) prepared via a very simple green preparation method. An aqueous leaves extract of Moringa oleifera was used to obtain the bimetallic Ag@Au/CNC nanocomposite. High-resolution transmission electron microscopy (HRTEM) observations revealed the successful formation of triangle, hexagonal, and spherical shapes of well-combined Ag-Au nanoparticles on the regenerated cellulose nanofiber surface. Further, the formation of Au-Ag bimetallic nanostructures was confirmed by X-ray photoelectron spectroscopy (XPS) and X-ray crystallography (XRD) results. The resultant bimetallic Ag@Au/CNC catalyst was found to perform remarkably well in the reduction of nitrophenols. The bimetallic Ag@Au/CNC catalyst gave excellent kapp values of 15.59 and 22.83 × 10-3 s-1 for the 2- A nd 4-nitrophenol reduction process, respectively. To our delight, the Ag@Au/CNC catalyst was found to perform well in the aza-Michael reaction. The catalytic activity of Ag@Au/CNCs was compared with mono-metallic Ag/CNCs, Au/CNCs, and other reported catalysts. Based on the results obtained, the high synergy of Ag@Au/CNCs was explained. A possible mechanism is proposed for the Ag@Au/CNC-catalyzed nitrophenol reduction and aza-Michael reactions.

1,2-DIHYDRO-1-OXOPHTHALAZINYL DERIVATIVES HAVING BIOLOGICAL ACTIVITY ON SEROTONIN RECEPTORS 5-HT2A AND 5-HT2C, AND PREPARATION THEREOF

The present invention relates to a novel 1,2-dihydro-1-oxophthalazinyl piperazine compound having biological activity as serotonin receptor antagonist, a preparation method of the compound and a pharmaceutical composition for the treatment and prevention of central nervous system diseases comprising the compound.

Samarium(III) triflate catalyzed conjugate addition of amines to electron-deficient alkenes

Amines undergo smooth nucleophilic addition to α,β-unsaturated compounds in the presence of a catalytic amount of samarium(III) triflate at ambient temperature to produce the corresponding β-amino compounds in excellent yields. This method is simple, convenient, and works efficiently under mild conditions. Georg Thieme Verlag Stuttgart.