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Usage

Uses

Used in Organic Synthesis:
2,3-bis[(4-methylphenyl)sulfanyl]naphthalene-1,4-dione is used as a key intermediate in the synthesis of various organic compounds, particularly in the field of photochromic materials and dyes. Its unique structure allows for the development of novel materials with reversible color changes upon exposure to light, making it valuable for applications such as smart windows, optical data storage, and sensors.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, 2,3-bis[(4-methylphenyl)sulfanyl]naphthalene-1,4-dione is utilized as a building block for the development of new drugs. Its chemical properties and reactivity make it a promising candidate for the synthesis of therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Agrochemical Production:
2,3-bis[(4-methylphenyl)sulfanyl]naphthalene-1,4-dione is also employed in the agrochemical sector for the production of pesticides and other crop protection agents. Its unique chemical structure can be leveraged to create novel compounds with enhanced efficacy and selectivity, contributing to more sustainable and effective agricultural practices.
Used in Antioxidant and Anti-inflammatory Research:
Due to its potential antioxidant and anti-inflammatory properties, 2,3-bis[(4-methylphenyl)sulfanyl]naphthalene-1,4-dione is being studied for its potential use in the development of therapeutic agents targeting oxidative stress and inflammation-related disorders. Its sulfur-containing aromatic structure may contribute to its ability to modulate cellular processes and protect against tissue damage.

Upstream product

• 117-80-6 2,3-Dichloro-1,4-naphthoquinone 
• 106-45-6 para-thiocresol 
• 130-15-4 [1,4]naphthoquinone 
• 1099739-80-6 2,3-di-(4-methylphenyl)sulphanyl-1,4-naphthalenediol 

Relevant academic research and scientific papers

Synthesis, biological, and computational study of naphthoquinone derivatives containing heteroatoms

A number of 2-(aryl/alkyl)thio-3-chloro-l,4-naphthoquinones (3a-g) and 2,3-(aryl/alkyl)thio-l,4-naphthoquinones (4a-d, 4f-g) were obtained by the reactions of 2,3-dichloro-1,4-naphthoquinone (1) with some various thiols and subsequently used as building b

Polymorphs of aromatic thiolato 1, 2 or 1,4-naphthoquinones

Two polymorphs of 4-(phenylthio)naphthalene-1,2-dione have been shown to possess distinguishable C-H...O hydrogen bond interactions; on the other hand two polymorphs of 2,3-(bis-4-methylphenylsulfanyl)naphthalene-1,4-dione have different orientations of m

Synthesis of mixed aryl 2,3-diarylsulphanyl-1,4-naphthoquinones

The reaction of 2-arylsulphanyl-1,4-napththoquinone with aromatic thiols and sodium dithionate leads to bis-2,3-(arylsulphanyl)naphthalene-1,4-diols in high yield. Corresponding oxidized products, namely 2,3-diarylsulphanyl-1,4- naphthoquinones, are prepa

Synthesis and?evaluation of?antifungal activity of?naphthoquinone derivatives

3-Arylamino-2-phenylsulfinylnaphthoquinones, 2,3-diarylthio-naphthoquinones and 2-phenylsulfinyl-3-arylthio-1,4-dihydronaphtalenes are synthesized and tested against five fungi. The activities of these products were better than amphotericine B against all

Synthesis of benzo[b]naphtho[2,3-d]thiophene-6,11-diones via palladium(II) acetate-mediated cyclization of 3-arylthio-1,4-naphthoquinone

Palladium(II)-mediated oxidative cyclization of 3-arylthio-1,4- naphthoquinone (4) giving biologically important benzo[b]naphtho-[2,3-d] thiophene-6,11-diones (2) has been performed with a stoichiometric amount of palladium(II) acetate in distillated acet