6302-91-6

Usage

Physical state

Colorless liquid 2-(4-chlorophenyl)-2-methyl-1,3-dithiolane is a liquid that appears colorless, meaning it does not have any visible color.

Odor

Strong, unpleasant The compound has a strong and unpleasant odor, which can be detected at low concentrations.

Uses

Intermediate in synthesis 2-(4-chlorophenyl)-2-methyl-1,3-dithiolane is used as an intermediate in the production of pharmaceuticals and agricultural chemicals, meaning it is a key component in the synthesis of other compounds.

Flavoring agent

Food industry 2-(4-chlorophenyl)-2-methyl-1,3-dithiolane is also used as a flavoring agent in the food industry, adding taste and aroma to various food products.

Potential applications

Insecticidal and antifungal properties 2-(4-chlorophenyl)-2-methyl-1,3-dithiolane has been studied for its potential to act as an insecticide and antifungal agent, which could be useful in controlling pests and fungi in various settings.

Safety concerns

Harmful if ingested, inhaled, or in contact with skin It is important to handle 2-(4-chlorophenyl)-2-methyl-1,3-dithiolane with care, as it can cause harm if it is ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken when working with this chemical.

Upstream product

• 99-91-2 para-chloroacetophenone 
• 540-63-6 ethane-1,2-dithiol 

Downstream Products

• 622-98-0 4-chloro(ethylbenzene) 
• 6317-12-0 5-(4-chlorophenyl)-2,3-dihydro-1,4-dithiine 
• 99-91-2 para-chloroacetophenone 

Relevant academic research and scientific papers

PhIO-Mediated oxidative dethioacetalization/dethioketalization under water-free conditions

Treatment of thioacetals and thioketals with iodosobenzene in anhydrous DCM conveniently afforded the corresponding carbonyl compounds in high yields under water-free conditions. The mechanistic studies indicate that this dethioacetalization/dethioketalization process does not need water and the oxygen of the carbonyl products comes from the hypervalent iodine reagent.

Silica-gel supported sulfamic acid (SA/SiO2) as an efficient and reusable catalyst for conversion of ketones into oxathioacetals and dithioacetals

A simple and efficient method for the conversion of carbonyl compounds to oxathioacetals and dithioacetals using SA/SiO2 as an acid catalyst has been achieved. SA/SiO2 is easily recovered from the reaction mixture and can be reused at least 15 times without loss of catalytic activity.

Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide as a mild and efficient catalyst for chemoselective thioacetalization of carbonyl functions and transthioacetalization reactions

Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide are effective catalysts for chemoselective dithioacetalization of aldehydes in the presence of ketones under neutral conditions.

Silica-PCl5: A novel heterogenous catalyst for simple and efficient chemoselective protection of carbonyl compounds

A simple, efficient and environmentally benign procedure has been developed for chemoselective protection of carbonyl compounds using the newly developed heterogeneous catalyst: Silica-PCl5. A variety of aldehydes and ketones were efficiently c

An efficient, continuous flow technique for the chemoselective synthesis of thioacetals

By optimizing a reagent's residence time within a packed-bed reactor, it is possible to overcome selectivity issues frequently encountered in stirred reaction vessels. This important feature is demonstrated for the chemoselective protection of 4-acetylben

An efficient method for thioacetalization of carbonyl compounds in the presence of a catalytic amount of benzyltriphenylphosphonium tribromide under solvent-free conditions

A variety of carbonyl compounds have been successfully converted to the corresponding thioacetal derivatives in good to excellent yields on the reaction of carbonyl compounds with 1,2-ethanedithiole, 1,3-propanedithiol, and ethanethiol in the presence of

Chemoselective dithioacetalization of aldehydes using silica sulfuric acid as a reusable catalyst

Silica sulfuric acid has been found to be an efficient and reusable catalyst for chemoselective dithioacetalization of aldehydes over ketones, in excellent yields.

A simple and efficient heterogeneous procedure for thioacetalization of aldehydes and ketones

A new procedure for the protection of aldehydes and ketones as thioacetals promoted by catalytic amount of p-toluene-sulfonic acid and silica gel has been developed. This procedure offers versatility, short reaction time, excellent yield, good selectivity

Ruthenium(III) chloride-catalyzed thioacetalization of carbonyl compounds: Scope, selectivity, and limitations

A variety of carbonyl compounds can be easily and rapidly converted to the corresponding cyclic and acylic dithioacetals in the presence of a catalytic amount of ruthenium chloride in acetonitrile at room temperature. Some of the major advantages of this