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Usage

Uses

Used in Organic Synthesis:
2-(2,4-dichlorophenyl)-1,3-dithiolane is used as a building block in the synthesis of heterocyclic compounds, which are important in various chemical and pharmaceutical applications due to their diverse and biologically active structures.
Used in Pharmaceutical Production:
As a synthetic intermediate, 2-(2,4-dichlorophenyl)-1,3-dithiolane contributes to the manufacturing process of pharmaceuticals, playing a crucial role in the development of new drugs and medicinal compounds.
Used in Agrochemical Production:
2-(2,4-dichlorophenyl)-1,3-dithiolane is also utilized as a synthetic intermediate in the production of agrochemicals, specifically in the creation of pesticides and other agricultural chemicals that protect crops and enhance yield.
Used in Antimicrobial Applications:
2-(2,4-dichlorophenyl)-1,3-dithiolane has been studied for its potential antimicrobial properties, suggesting its use in applications that require the inhibition of microbial growth, such as in medical or industrial settings.
Used as an Antioxidant:
2-(2,4-dichlorophenyl)-1,3-dithiolane's potential antioxidant properties indicate its use in applications where protection against oxidative damage is necessary, such as in the food industry or in cosmetic products.
Used in Agricultural Fungicides:
2-(2,4-dichlorophenyl)-1,3-dithiolane has been examined for its use as a fungicide in agriculture, helping to control fungal infections in crops and thereby improving agricultural productivity.
Used in Chemical Research:
Due to its unique structure and properties, 2-(2,4-dichlorophenyl)-1,3-dithiolane is also utilized in chemical research for studying the synthesis and reactions of organosulfur compounds and their potential applications in various fields.

InChI:InChI=1/C9H8Cl2S2/c10-6-1-2-7(8(11)5-6)9-12-3-4-13-9/h1-2,5,9H,3-4H2

Upstream product

• 874-42-0 2,4-dichlorobenzaldeyhde 
• 540-63-6 ethane-1,2-dithiol 
• 13086-94-7 1,1-diacetoxy-1-(2,4-dichlorophenyl)methane 

Relevant academic research and scientific papers

Visible-light promoted dithioacetalization of aldehydes with thiols under aerobic and photocatalyst-free conditions

A novel photocatalyst-free visible-light-mediated dithioacetalization of aldehydes and thiols has been developed. This protocol is operationally simple, mild and atom-economical, which provides an environmental benign access to dithioacetals at room temperature under aerobic conditions.

Aluminum hydrogen sulfate [Al(HSO4)3] as an efficient catalyst for the preparation of thioacetals

Aluminum hydrogen sulfate, as a heterogeneous solid acid catalyst, has been used for the mild conversion of carbonyl compounds to their thioacetals using 1,2- and 1,3-dithiol under ambient conditions with short reaction times in high to excellent yield in

An efficient method for the transthioacetalization of acylals and acetals under mild conditions

A rapid and efficient method for the transthioacetalization of acylals (1,1-diacetates) and acyclic and cyclic acetals is described. The reaction was carried out using 1-benzyl-4-aza-1-azoniabicyclo[2.2.2]octane tribromide (1 mol%). The yield of the transthioacetalization was high and reaction conditions involve the use of acetonitrile as the solvent at room temperature; isolation is simple and the products are nearly pure.

Chemoselective dithioacetalization of carbonyl compounds using magnesium hydrogensulfate as efficient heterogeneous catalyst

Carbonyl compounds have been successfully converted into their corresponding dithiolanes and dithianes derivatives with 1,2-ethanedithiol and 1,3-propanedithiol in excellent yield at room temperature and short reaction times using a catalytic amount of ma

A facile and efficient procedure for the transdithioacetalization of 1,1-diacetates using POCl3-montmorillonite as catalyst

A rapid and efficient method for the transdithioacetalization of 1,1-diacetates with 1,2-dithioglycol was described in good to excellent yield catalyzed by POCl3-montmorillonite.

A rapid and efficient method of thioacetalization of carbonyl compounds catalysed by POCl3-montmorillnite

Aldehydes and ketones were thioactalized with 1,2-ethanedithiol in the presence POCl3-montmorillonite at room temperature in excellent yields.

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.