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3-[(4-phenylpiperazin-1-yl)methyl]-1H-indole is a complex organic compound with a molecular formula of C21H22N4. It is characterized by an indole ring system, which is a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. The compound features a 4-phenylpiperazine moiety, which is a piperazine ring with a phenyl group attached at the 4-position. The phenylpiperazine is connected to the indole through a methylene bridge (-CH2-). This specific arrangement of atoms and functional groups gives the compound its unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

4281-72-5

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4281-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4281-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4281-72:
(6*4)+(5*2)+(4*8)+(3*1)+(2*7)+(1*2)=85
85 % 10 = 5
So 4281-72-5 is a valid CAS Registry Number.

4281-72-5SDS

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 3-((4-phenylpiperazin-1-yl)methyl)-1H-indole

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4281-72-5 SDS

4281-72-5Downstream Products

4281-72-5Relevant academic research and scientific papers

Synthetic indole Mannich bases: Their ability to modulate in vitro cellular immunity

Mesaik, M. Ahmed,Khan, Khalid Mohammed,Rahim, Fazal,Taha, Muhammad,Haider, Syed Moazzam,Perveen, Shahnaz,Khalid, Ahmed Shukralla,Abdalla, Omer M.,Soomro, Samreen,Voelter, Wolfgang

, p. 118 - 122 (2015/06/02)

The synthetic indole Mannich bases 1-13 have been investigated for their ability to modulate immune responses measured in vitro. These activities were based on monitoring their affects on T-lymphocyte proliferation, reactive oxygen species (ROS), IL (inte

An efficient eco-friendly synthesis of Indole-Mannich base

Khan, Khalid Mohammed,Rahim, Fazal,Ambreen, Nida,Taha, Muhammad,Iqbal, Sarosh,Haider, Syed Moazzam,Perveen, Shahnaz

experimental part, p. 748 - 757 (2012/08/07)

An efficient and simplified protocol for three component Mannich reaction of indoles in water without using any catalyst is described. Different functionalized indole Mannich base synthesized in relatively short time with moderate to good yields. The adva

Design, synthesis, and biological evaluation of indole-based 1,4-disubstituted piperazines as cytotoxic agents

Akkoc, Meric Koeksal,Yueksel, Mine Yarim,Durmaz, Irem,Atalay, Renguel Ecetin

experimental part, p. 515 - 525 (2012/09/22)

A series of 3-[(4-substitutedpiperazin-1-yl)methyl]-1H -indole derivatives were synthesized, and their structures were confirmed by spectral analysis. All the compounds were tested for their cytotoxic activity in vitro against 3 human tumor cell lines: human liver (HUH7), breast (MCF7), and colon (HCT116). Among the designed derivatives, most of the compounds showed significant cytotoxicity against liver and colon cancer cell lines with lower IC50 concentrations than the standard drug 5-fluorouracil. Compound 3s, with 3,4-dichlorophenyl substituent on the piperazine ring, was the most active in suppressing the growth of all screened cancer cells. TUeBITAK.

Indole mannich bases and their antimycobacterial effect

Malinka, Wieslaw,Swiatek, Piotr

, p. 107 - 111 (2007/10/03)

3-[(4-arylpiperazin-1-yl)methyl]indoles (2a-h) and 3-[(4-hydroxy-4- phenylpiperazin-1-yl)methyl]indole (3) were prepared and characterized by 1H NMR and mass spectrometry. All eight compounds (2a-c, e-h and 3) tested inhibited in vitro the growth of Mycobacterium tuberculosis H 37Rv in the range of 98-7% at a concentration of ≥ 6.25 μg/ml. From the preliminary microbiological data it is possible to observe that a simple increasing of lipophilicity of the compounds tested to above logP calc. ≥3.8 significantly increases the potencies of their antitubercular action.

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