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2-PIPERAZINE-1-YL-ACETAMIDE is a chemical compound characterized by the molecular formula C6H13N3O. It is a white crystalline solid that exhibits solubility in both water and organic solvents. This versatile compound is primarily utilized as an intermediate in the pharmaceutical industry, playing a crucial role in the synthesis of various heterocyclic compounds. Its pharmacological activities have positioned it as a potential candidate for drug development, with studies highlighting its potential as an anti-cancer, anti-inflammatory, anti-bacterial agent, and central nervous system depressant. Furthermore, it is being investigated for its potential therapeutic applications in treating neurological disorders.

55829-43-1

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55829-43-1 Usage

Uses

Used in Pharmaceutical Industry:
2-PIPERAZINE-1-YL-ACETAMIDE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of heterocyclic compounds, which are integral in the development of new drugs.
Used in Anti-Cancer Applications:
2-PIPERAZINE-1-YL-ACETAMIDE is used as a potential anti-cancer agent due to its pharmacological properties that may contribute to the inhibition of cancer cell growth and proliferation.
Used in Anti-Inflammatory Applications:
As an anti-inflammatory agent, 2-PIPERAZINE-1-YL-ACETAMIDE is utilized for its potential to reduce inflammation, a common characteristic in various diseases and conditions.
Used in Anti-Bacterial Applications:
2-PIPERAZINE-1-YL-ACETAMIDE is used as a potential anti-bacterial agent, indicating its possible role in combating bacterial infections.
Used in Central Nervous System Depressant Applications:
2-PIPERAZINE-1-YL-ACETAMIDE is used as a central nervous system depressant, suggesting its potential in managing conditions that involve overactivity of the central nervous system.
Used in Neurological Disorder Treatment:
2-PIPERAZINE-1-YL-ACETAMIDE is being investigated for its potential use in the treatment of various neurological disorders, highlighting its possible therapeutic benefits in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 55829-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55829-43:
(7*5)+(6*5)+(5*8)+(4*2)+(3*9)+(2*4)+(1*3)=151
151 % 10 = 1
So 55829-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N3O.2ClH.H2O/c7-6(10)5-9-3-1-8-2-4-9;;;/h8H,1-5H2,(H2,7,10);2*1H;1H2

55829-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Piperazin-1-yl-acetic acid

1.2 Other means of identification

Product number -
Other names 2-PIPERAZINE-1-YL-ACETAMIDE

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:55829-43-1 SDS

55829-43-1Relevant academic research and scientific papers

ISOXAZOLE CARBOXAMIDE COMPOUNDS AND USES THEREOF

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Page/Page column 66, (2020/04/25)

A compound of Formula (I) or or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating hearing loss or balance disorder: Formula (I) wherein R1 and Y are as defined herein.

CHEMICAL COMPOUNDS

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Page/Page column 108-109, (2010/10/20)

The present invention provides novel compounds that demonstrate protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor, and which affect the binding of the natural ligand or chemokine to a receptor such as CXCR4 and/or CCR5 of a target cell.

Studies in Potential Filaricides: Part XV - Synthesis of 1-Acyl/Aryl-4-substituted-piperazines as Diethylcarbamazine Analogs

Agrawal, V. K.,Sharma, Satyavan

, p. 650 - 654 (2007/10/02)

1-Acyl-4-substituted-piperazines (4-29) have been prepared starting from 1-benzylpiperazine while 1-aryl-4-aroylpiperazines (30-44) have been obtained from the corresponding 1-arylpiperazines.None of the compounds shows any significant filaricidal activity against Litomosoides carinii in cotton rats and cestodicial activity against Hymenolepis nana in mice.

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