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3H-1,2-Dithiol-3-one, 5-(4-methoxyphenyl)- is a chemical compound with the molecular formula C9H8OS2. It is a derivative of 1,2-dithiol-3-one, featuring a 4-methoxyphenyl group attached to the 5-position. 3H-1,2-Dithiol-3-one, 5-(4-methoxyphenyl)- is characterized by the presence of a 3H-1,2-dithiol-3-one core, which consists of a sulfur atom bonded to a carbonyl group (C=O) and another sulfur atom, forming a cyclic structure. The 4-methoxyphenyl group adds a methoxy (-OCH3) functional group to the para position of the phenyl ring, which can influence the compound's reactivity and physical properties. This chemical is primarily used in research and development, particularly in the synthesis of various organic compounds and as a building block in the preparation of pharmaceuticals and other specialty chemicals.

831-30-1

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831-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 831-30-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 831-30:
(5*8)+(4*3)+(3*1)+(2*3)+(1*0)=61
61 % 10 = 1
So 831-30-1 is a valid CAS Registry Number.

831-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(p-methoxyphenyl)dithia[1,2]cyclopenten-3-one

1.2 Other means of identification

Product number -
Other names 3-Oxo-5-[4-methoxy-phenyl]-3H-[1,2]dithiol

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:831-30-1 SDS

831-30-1Relevant academic research and scientific papers

DESMETHYLANETHOLE TRITHIONE DERIVATIVES FOR THE TREATMENT OF DISEASES LINKED TO MITOCHONDRIAL REACTIVE OXYGEN SPECIES (ROS) PRODUCTION

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Page/Page column 84; 88, (2018/09/28)

The present invention relates to desmethylanethole trithione ( AOX ) and derivatives thereof, especially derivatives of formula (I), for the prevention and treatment of diseases whose initiation and/or evolution relates to the production and effects of re

Metabolism of anethole dithiolethione by rat and human liver microsomes: Formation of various products deriving from its o-demethylation and s-oxidation. Involvement of cytochromes P450 and flavin monooxygenases in these pathways

Dulac, Martin,Sassi, Amor,Nagarathinan, Citra,Christen, Marie-Odile,Dansette, Patrick M.,Mansuy, Daniel,Boucher, Jean-Luc

, p. 1390 - 1395 (2018/09/13)

A study of the metabolism of anethole dithiolethione (ADT, 5-(p-methoxyphenyl)-3H-1,2-dithiole-3-thione) by rat and human liver microsomes showed the formation of the corresponding S-oxide and the S-oxide of desmethyl-ADT (dmADT, 5-(p-hydroxyphenyl)-3H-1,

SYNTHESIS OF SUBSTITUTED THIENOTHIAZOLES AND INDOLOTHIAZOLES

Pinkin, L. D.,Dzyubenko, V. G.,Abramenko, P. I.,Shpileva, I. P.

, p. 345 - 352 (2007/10/02)

Alkylene-, halo-, and aryl-substituted 2-methylthienothiazoles were obtained by the action of phosphorus pentasulfide on the corresponding 2-acetylamino-3-bromo- or 2-acetylamino-3-hydroxythiophenes in an organic solvent with heating. 2-Oximes of halo- and methyl-substituted isatins were converted by reduction and acetylation into 2-hydroxy-3-acetylaminoindoles, from which 2-methylindolo-thiazoles were obtained by the action of phosphorous pentasulfide with heating in xylene.

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