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3-[4-(4-Methoxyphenyl)piperazin-1-yl]propan-1-amine is a complex organic compound belonging to the phenylpiperazine class. It features a piperazine ring connected to a phenyl group, with a methoxy group attached to the phenyl and an amine group linked to a propane chain. As a derivative of piperazine, 3-[4-(4-METHOXYPHENYL)PIPERAZIN-1-YL]PROPAN-1-AMINE may possess pharmacological properties, although its specific uses, toxicity, and safety profile are not well documented and necessitate further scientific investigation. Careful handling following standard safety protocols is essential when working with such compounds.

40255-50-3

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40255-50-3 Usage

Uses

Used in Pharmaceutical Industry:
3-[4-(4-Methoxyphenyl)piperazin-1-yl]propan-1-amine is used as a potential active pharmaceutical ingredient for its possible pharmacological properties. Its exact applications in medicine are yet to be determined, but as a phenylpiperazine derivative, it may be explored for its potential effects on the central nervous system or other therapeutic areas.
Used in Chemical Research:
In the field of chemical research, 3-[4-(4-Methoxyphenyl)piperazin-1-yl]propan-1-amine serves as a subject for studying the structure-activity relationships of phenylpiperazine compounds. Its unique structure may provide insights into the development of new drugs or the understanding of molecular interactions within biological systems.
Used in Material Science:
Although not explicitly mentioned in the provided materials, due to its amine and methoxy groups, 3-[4-(4-Methoxyphenyl)piperazin-1-yl]propan-1-amine could potentially be used in material science for the development of new polymers or as a component in the synthesis of other complex organic materials, given its ability to form various types of chemical bonds.

Check Digit Verification of cas no

The CAS Registry Mumber 40255-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,5 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40255-50:
(7*4)+(6*0)+(5*2)+(4*5)+(3*5)+(2*5)+(1*0)=83
83 % 10 = 3
So 40255-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H23N3O/c1-18-14-5-3-13(4-6-14)17-11-9-16(10-12-17)8-2-7-15/h3-6H,2,7-12,15H2,1H3/p+2

40255-50-3SDS

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-(4-methoxyphenyl)piperazin-1-yl]propan-1-amine

1.2 Other means of identification

Product number -
Other names 3-(4-(4-methoxyphenyl)-1-piperazinyl)propylamine

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:40255-50-3 SDS

40255-50-3Relevant academic research and scientific papers

KAPPA OPIOID RECEPTOR EFFECTORS AND USES THEREOF

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Paragraph 00052, (2013/03/28)

The present invention is a selective kappa opioid receptor effector, or a pharmaceutically acceptable salt thereof, useful for treating ethanol use disorder withdrawal, anxiety and/or depression, schizophrenia, mania or post-traumatic stress disorder.

Synthesis and biological evaluation of oxazole derivatives as T-type calcium channel blockers

Lee, Jie Eun,Koh, Hun Yeong,Seo, Seon Hee,Baek, Yi Yeon,Rhim, Hyewhon,Cho, Yong Seo,Choo, Hyunah,Pae, Ae Nim

scheme or table, p. 4219 - 4222 (2010/09/04)

T-type calcium channel is one of therapeutic targets for the treatment of cardiovascular diseases and neuropathic pain. In this study, as a part of our ongoing efforts to develop potent T-type calcium channel blockers, we designed oxazole derivatives subs

POTENTIAL NEUROLEPTICS OF THE ORTHOPRAMIDE SERIES; SYNTHESIS OF N-(3-(TERT.AMINO)PROPYL)-5-SULFAMOYL-2-METHOXYBENZAMIDES

Valenta, Vladimir,Vlkova, Marie,Holubek, Jiri,Svatek, Emil,Metysova, Jirina,Protiva, Miroslav

, p. 797 - 808 (2007/10/02)

Heating ethyl 5-sulfamoyl-2-methoxybenzoate with a series of twelve 3-(tert.amino)propylamines (IIIa-IIIl) afforded the title compounds IIa-IIl which were transformed to salts and subjected to pharmacological screening as potential neuroleptics of the sulpiride series.Only compounds IId (hydrogen oxalate, VUFB-15 453) and IIg (methanesulfonate, VUFB-15 397) showed indications of the desired psychotropic activity.

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