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1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)-4-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82991-94-4

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82991-94-4 Usage

Molecular Structure

Consists of a dithiole ring and a methoxyphenyl group

Antioxidant

May help protect cells from damage caused by free radicals

Anti-inflammatory

May reduce inflammation in the body

Anti-cancer

Potentially inhibits the growth of cancer cells

Cognitive Function

Investigated for its potential to improve cognitive function

Neurodegenerative Disease Protection

May protect against diseases like Alzheimer's and Parkinson's

Diabetes Treatment

Shown promise in the treatment of diabetes

Cardiovascular Disease Treatment

Potentially beneficial in treating cardiovascular diseases

Further Research

More research is needed to fully understand the therapeutic potential of 1,3-Dithiole, 2-(1,3-dithiol-2-ylidene)-4-(4-methoxyphenyl)-

Scientific Interest

Garnered significant interest in the scientific community for its diverse range of potential medical applications

Check Digit Verification of cas no

The CAS Registry Mumber 82991-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,9 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82991-94:
(7*8)+(6*2)+(5*9)+(4*9)+(3*1)+(2*9)+(1*4)=174
174 % 10 = 4
So 82991-94-4 is a valid CAS Registry Number.

82991-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,3-dithiol-2-ylidene)-4-(4-methoxyphenyl)-1,3-dithiole

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:82991-94-4 SDS

82991-94-4Downstream Products

82991-94-4Relevant academic research and scientific papers

Selective Functionalization of Tetrathiafulvalene Using Mg- and Zn-TMP-Bases: Preparation of Mono-, Di-, Tri-, and Tetrasubstituted Derivatives

Nafe, Julia,Auras, Florian,Karaghiosoff, Konstantin,Bein, Thomas,Knochel, Paul

supporting information, p. 5356 - 5359 (2015/11/18)

The tetrathiafulvalene-scaffold (TTF) reacts selectively in allylation, acylation, arylation, halogenation, and thiolation reactions via magnesium or zinc derivatives that are obtained by a direct metalation with Mg- and Zn-TMP-bases (TMP = 2,2,6,6-tetram

Palladium-catalysed Coupling of Trialkylstannyltetrathiafulvalenes with Aryl Halides

Iyoda, Masahiko,Kuwatani, Yoshiyuki,Ueno, Nobuhiko,Oda, Masaji

, p. 158 - 159 (2007/10/02)

Trialkylstannyltetrathiafulvalenes undergo palladium-catalysed cross- and homo-coupling reactions to give aryl-substituted tetrathiafulvalenes and bitetrathiafulvalene; the methodology has been applied to the synthesis of p-phenylenebistetrathiafulvalene

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