59057-35-1

Usage

Uses

Used in Pharmaceutical Synthesis:
2,4,6-Trimethylbenzenesulfinic acid serves as a crucial chemical intermediate in the production of pharmaceuticals. Its role in the synthesis process is pivotal for creating a range of medicinal compounds that address various health conditions.
Used in Agrochemical Production:
In the agrochemical industry, 2,4,6-trimethylbenzenesulfinic acid is utilized for the synthesis of various agrochemicals. Its contribution to this field helps in developing products that enhance crop protection and contribute to sustainable agriculture.
Used in Dye Manufacturing:
2,4,6-trimethylbenzenesulfinic acid is also integral to the dye industry, where it is used in the synthesis of different types of dyes. Its presence in this application allows for the creation of dyes with specific color characteristics and properties.
Used as a Reducing Agent in Organic and Bioorganic Chemistry:
2,4,6-Trimethylbenzenesulfinic acid acts as a reducing agent, playing a significant role in organic and bioorganic chemistry. Its reducing properties facilitate various chemical reactions that are essential in the synthesis of complex organic molecules.
Used in the Conversion of Carbonyl Compounds:
As a versatile reagent, 2,4,6-trimethylbenzenesulfinic acid is instrumental in the conversion of carbonyl compounds to their corresponding oximes. This transformation is vital for the synthesis of pharmaceuticals and fine chemicals, which are used in a wide array of applications.
Used in Polymer Production:
2,4,6-trimethylbenzenesulfinic acid finds use in the manufacturing of polymers, where it contributes to the development of materials with specific properties. Its role in polymer chemistry is essential for creating innovative materials that meet various industrial needs.
Used as a Source of Sulfur Dioxide in Organic Reactions:
2,4,6-Trimethylbenzenesulfinic acid is also employed as a source of sulfur dioxide in certain organic reactions. Its ability to release sulfur dioxide under specific conditions makes it a valuable component in a range of chemical processes.

Upstream product

• 773-64-8 2-mesitylenesulphonyl chloride 
• 108-67-8 1,3,5-trimethyl-benzene 
• 3112-79-6 dimesityl sulfone 
• 71-43-2 benzene 
• 82965-02-4 hexyl 2,4,6-trimethylbenzenesulfonate 

Downstream Products

• 59057-21-5 1,3,5-Trimethyl-2-[(2E,4E)-3-methyl-5-(2,6,6-trimethyl-cyclohex-1-enyl)-penta-2,4-diene-1-sulfonyl]-benzene 
• 135216-98-7 2,4,6-trimethylphenyl 1-methyl-4-nitro-5-imidazolyl sulfone 
• 1483-92-7 bis(2,4,6-trimethylphenyl)disulfide 
• 73766-65-1 2,4,6-trimethylbenzenesulfinyl chloride 
• 59057-28-2 Acetic acid (2E,6E,8E)-3,7-dimethyl-5-(2,4,6-trimethyl-benzenesulfonyl)-9-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-2,6,8-trienyl ester 
• 73766-66-2 S_S-l-menthyl 2,4,6-trimethylbenzenesulfinate 
• 73766-51-5 R_S-l-menthyl 2,4,6-trimethylbenzenesulfinate 
• 73766-54-8 (+)-(R)-(1-Cyclohexenylmethyl)-mesityl-sulfoxid 
• 73766-53-7 (-)-(R)-(Cyclohexylidenmethyl)-mesityl-sulfoxid 
• 253316-09-5 (RS)-N-[carbo-(1R)-menthoxy]-2,4,6-trimethylbenzenesulfonimidoyl chloride 
• 137280-44-5 methyl 2,4,6-trimethylbenzenesulphinate 
• 137280-46-7 ethyl 2,4,6-trimethylbenzenesulphinate 
• 39153-60-1 S-mesityl 2,4,6-trimethylbenzenesulfonothioate 
• 6462-31-3 methyl 2,4,6-trimethylphenyl sulfone 

Relevant academic research and scientific papers

Palladium-catalyzed desulfitative heck-type reaction of aryl sulfinic acids with alkenes

An efficient protocol has been developed for the desulfitative Heck-type reaction of aryl sulfinic acids with a variety of alkenes in the presence of a catalytic amount of Pd(OAc)2 and inexpensive Cu(OAc)2 as oxidant. This method does not require a ligand or a base, thereby broadening the scope of Pd-catalyzed coupling reactions. Copyright

Nitrosations with hydrazine derivatives: Synthesis of N4-arenesulfinylsemicarbazides and N5-arenesulfinyl-N1-aminobiuretes from arenesulfinylisocyanates and N,N-disubstituted hydrazines

Arenesulfinyl-isocyanates 5 prepared in situ from arenesulfinyl chlorides 4 and silver cyanate react with N,N-disubstituted hydrazines to mixtures of N4-arenesulfinylsemicarbazides 6 as main components and N5-arenesulfinyl-N1/s

STUDIEN ZUM VORGANG DER WASSERSTOFFUEBERTRAGUNG 64. ELECTROREDUCTIVE SPALTUNG VON ARYLSULFONSAEUREDERIVATEN UND ARYLSULFONEN MIT ALKALI-AMALGAMEN

Arylsulfonylchlorides, n-hexylarylsulfonates and di-aryl sulfones (ArSO2Y; Y=Cl, OC6H13, Ar') were cleaved under standard conditions by alkali metal amalgams (M/Hg; M=Li, Na, K) to the corresponding sulfinate salts (ArSO2M) and MY, as shown in Eq. 1.The substrates ArSO2Y in toluene were not cleaved by Li/Hg alone; first on addition of an equimolar amount of i-propanol could conversions of almost 100percent be achieved. (Tables I,II,III).A series of six n-hexylarylsulfonates were studied under standard conditions, to establish the influence of the reaction medium and the amalgam on the course of reaction, (Table II).The sterically hindered arylsulfonates ArSO2OC6H13, (Ar= mesityl, 2,4,6-tri-isopropyl) were "anomalous", i.e. underwent fission at the ring/sulfur bond , as shown by Eq. 2.Table III describes the reductive fission of mesityl-phenylsulfone and dimesitylsulfone.