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1,3-Dithiole-2-thione, 4-methyl-5-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83363-15-9

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83363-15-9 Usage

Molecular weight

178.31 g/mol

Structure

A sulfur-containing compound with a 1,3-dithiole core, featuring a thione group (C=S) at position 2, a methyl group at position 4, and a 4-methylphenyl group at position 5.

Family

Dithiolethiones

Antioxidant

Exhibits antioxidant activity, potentially neutralizing harmful free radicals.

Anti-inflammatory

Demonstrates anti-inflammatory properties, which may help reduce inflammation in the body.

Cytoprotective

Offers protection to cells from various harmful agents or conditions.

Pharmaceutical

May have therapeutic potential in the development of drugs targeting various diseases.

Biological

Could be used in the study of biological processes and pathways related to its antioxidant, anti-inflammatory, and cytoprotective properties.

Therapeutic potential

Research suggests that 1,3-Dithiole-2-thione, 4-methyl-5-(4-methylphenyl)- may be useful in the treatment of conditions such as cancer, cardiovascular diseases, and neurodegenerative disorders.

Further investigation

Its structure and properties make it an interesting subject for additional research and potential drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 83363-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,6 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83363-15:
(7*8)+(6*3)+(5*3)+(4*6)+(3*3)+(2*1)+(1*5)=129
129 % 10 = 9
So 83363-15-9 is a valid CAS Registry Number.

83363-15-9Relevant academic research and scientific papers

Tetrathiafulvalenes. XVI. Spectroscopic and Electrical Properties of TTF and TTF-TCNQ-Complexes

Schukat, G.,Fanghaenel, E.,Chyla, A.

, p. 422 - 428 (2007/10/02)

UV-vis-spectra of mono- and dications of the TTF 2 show in comparison to those of TTF 1 and 3 that the aryl substituent in the TTF 2 is more twisted from the TTF-plane than in 1 and 3.Absorption maxima of mono- and dications of TTF 1 and 3 lie at a signif

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