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3-(4-ETHYL-PIPERAZIN-1-YL)-PROPYLAMINE is an organic chemical compound characterized by a piperazine ring with an ethyl group at the 4-position and a propylamine chain attached to the nitrogen atom. 3-(4-ETHYL-PIPERAZIN-1-YL)-PROPYLAMINE is recognized for its potential to bind with biological targets such as receptors and enzymes, making it a significant intermediate in the development of new therapeutic agents. Its structural features contribute to its utility in various applications across different industries.

4524-96-3

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4524-96-3 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-ETHYL-PIPERAZIN-1-YL)-PROPYLAMINE serves as a crucial building block for the synthesis of a range of drugs and bioactive molecules. Its presence in the composition of these pharmaceuticals is attributed to its ability to interact with biological targets, thereby playing a key role in the development of new therapeutic agents.
Used as a Ligand in Coordination Chemistry:
In the field of coordination chemistry, 3-(4-ETHYL-PIPERAZIN-1-YL)-PROPYLAMINE is utilized as a ligand. Its structural attributes allow it to form stable complexes with metal ions, which is vital for various applications, including catalysis and the creation of materials with specific properties.
Used as a Reagent in Organic Synthesis:
3-(4-ETHYL-PIPERAZIN-1-YL)-PROPYLAMINE also functions as a reagent in organic synthesis, facilitating a variety of chemical reactions. Its presence can enhance the efficiency of synthesis processes and contribute to the production of desired organic compounds.
Used in the Development of Therapeutic Agents for Neurological Disorders:
3-(4-ETHYL-PIPERAZIN-1-YL)-PROPYLAMINE has been investigated for its potential role in the treatment of neurological disorders. Its capacity to engage with specific biological targets makes it a promising candidate for the development of medications aimed at addressing such conditions.
Used in Cancer Treatment Research:
Furthermore, 3-(4-ETHYL-PIPERAZIN-1-YL)-PROPYLAMINE has been explored for its potential application in cancer treatment. Its interaction with biological targets suggests that it may contribute to therapeutic strategies against various types of cancer, offering new avenues for research and treatment development.

Check Digit Verification of cas no

The CAS Registry Mumber 4524-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,2 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4524-96:
(6*4)+(5*5)+(4*2)+(3*4)+(2*9)+(1*6)=93
93 % 10 = 3
So 4524-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H21N3/c1-2-11-6-8-12(9-7-11)5-3-4-10/h2-10H2,1H3

4524-96-3SDS

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 3-(4-ethylpiperazin-1-yl)propan-1-amine

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:4524-96-3 SDS

4524-96-3Downstream Products

4524-96-3Relevant academic research and scientific papers

[4-(Benzo[B]Thiophen-2-Yl) Pyrimidin-2-Yl]-Amine Derivatives As Ikk-Beta Inhibitors For The Treatment Of Cancer And Inflammatory Diseases

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Page/Page column 5, (2009/01/20)

The present invention provides compounds of Formula I: useful in the treatment of cancer and inflammatory diseases.

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