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1,3,3-trimethyl-2-[(E)-2-(4-nitrophenyl)ethenyl]-3H-indolium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5418-83-7

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5418-83-7 Usage

Chemical structure

1,3,3-trimethyl-2-[(E)-2-(4-nitrophenyl)ethenyl]-3H-indolium

Color

Deep blue

Applications

a. Dye for textiles
b. Medical applications

Uses

a. Antiseptic
b. Treatment for methemoglobinemia

Neuroprotective properties

Being researched for potential use in treating neurodegenerative diseases like Alzheimer's and Parkinson's

Other research areas

a. Anti-cancer agent
b. Treatment for malaria and other infectious diseases

Safety precautions

Can be toxic in high doses and may cause skin and eye irritation

Check Digit Verification of cas no

The CAS Registry Mumber 5418-83-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5418-83:
(6*5)+(5*4)+(4*1)+(3*8)+(2*8)+(1*3)=97
97 % 10 = 7
So 5418-83-7 is a valid CAS Registry Number.

5418-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,3-trimethyl-2-[2-(4-nitrophenyl)ethenyl]indol-1-ium,iodide

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:5418-83-7 SDS

5418-83-7Downstream Products

5418-83-7Relevant academic research and scientific papers

Disruption of mitochondrial redox homeostasis by enzymatic activation of a trialkylphosphine probe

Nguyen, Jade,Tirla, Alina,Rivera-Fuentes, Pablo

, p. 2681 - 2687 (2021/04/07)

Redox homeostasis is essential for cell function and its disruption is associated with multiple pathologies. Redox balance is largely regulated by the relative concentrations of reduced and oxidized glutathione. In eukaryotic cells, this ratio is different in each cell compartment, and disruption of the mitochondrial redox balance has been specifically linked to metabolic diseases. Here, we report a probe that is selectively activated by endogenous nitroreductases, and releases tributylphosphine to trigger redox stress in mitochondria. Mechanistic studies revealed that, counterintuitively, release of a reducing agent in mitochondria rapidly induced oxidative stress through accumulation of superoxide. This response is mediated by glutathione, suggesting a link between reductive and oxidative stress. Furthermore, mitochondrial redox stress activates a cellular response orchestrated by transcription factor ATF4, which upregulates genes involved in glutathione catabolism.

New mechanism, new chromophore: Investigating the electrophilic behaviour of styrylindolium dyes

Perry, Alexis

supporting information, p. 4825 - 4834 (2019/05/24)

To inform the design of future merocyanine-based sensors for nucleophilic analytes, a range of model styrylindolium salts were synthesised, and their behaviour towards cyanide, methanethiolate and sulfide was examined using spectroscopic techniques. In the majority of cases, standard 1,2-and 1,4-nucleophilic additions predominated; however, 4-nitrostyrylindolium salts underwent an unexpected dearomatising 1,8-addition with sulfur-centred nucleophiles. The enamine triene products thus produced display useful optical properties and provide a platform for novel sensor design, and the unusual 1,8-reaction pathway enables synthesis of novel molecular architecture.

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