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1-[3-(4-methylpiperazin-1-yl)propyl]-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70752-98-6

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70752-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70752-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,5 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70752-98:
(7*7)+(6*0)+(5*7)+(4*5)+(3*2)+(2*9)+(1*8)=136
136 % 10 = 6
So 70752-98-6 is a valid CAS Registry Number.

70752-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(4-methylpiperazin-1-yl)propyl]indole

1.2 Other means of identification

Product number -
Other names Piperazine,1-(3-(1-indolyl)propyl)-1-methyl

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:70752-98-6 SDS

70752-98-6Downstream Products

70752-98-6Relevant academic research and scientific papers

Synthesis and SAR evaluation of novel thioridazine derivatives active against drug-resistant tuberculosis

Scalacci, Nicolò,Brown, Alistair K.,Pavan, Fernando R.,Ribeiro, Camila M.,Manetti, Fabrizio,Bhakta, Sanjib,Maitra, Arundhati,Smith, Darren L.,Petricci, Elena,Castagnolo, Daniele

, p. 147 - 158 (2016/12/30)

The neuroleptic drug thioridazine has been recently repositioned as possible anti-tubercular drug. Thioridazine showed anti-tubercular activity against drug resistant mycobacteria but it is endowed with adverse side effects. A small library of thioridazine derivatives has been designed through the replacement of the piperidine and phenothiazine moieties, with the aim to improve the anti-tubercular activity and to reduce the cytotoxic effects. Among the resulting compounds, the indole derivative 12e showed an antimycobacterial activity significantly better than thioridazine and a cytotoxicity 15-fold lower.

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