66623-67-4

Usage

Uses

Used in Perfume Industry:
2,5-DIMETHYLTHIOANISOLE is used as a fragrance ingredient for its strong odor, contributing to the creation of various perfumes.
Used in Cosmetic Products:
2,5-DIMETHYLTHIOANISOLE is used as a flavoring agent and for adding scent to soaps and other cosmetic products, enhancing their appeal and sensory experience.
Used in Pharmaceutical Industry:
2,5-DIMETHYLTHIOANISOLE is used as an intermediate in the manufacture of pharmaceuticals, playing a crucial role in the synthesis of various organic compounds.
It is important to handle 2,5-DIMETHYLTHIOANISOLE with care, as it can be harmful if inhaled or ingested and may cause irritation to the eyes and skin.

Upstream product

• 4001-61-0 2,5-dimethylthiophenol 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 
• 624-92-0 Dimethyldisulphide 
• 106-42-3 para-xylene 

Downstream Products

• 187279-87-4 4-(2,5-dimethyl-4-methylthiophenyl)-4-ketobutanoic acid 
• 6462-29-9 (2,5-Dimethylphenyl) methyl sulfone 
• 187279-89-6 4-(2,5-dimethyl-4-methylthiophenyl)-4-ketobutanoyl-β-alanine benzyl ester 
• 156463-08-0 4-(2,5-dimethyl-4-methylthiophenyl)-4-hydroxybutanoyl-β-alanine 
• 187279-91-0 4-(2,5-dimethyl-4-methylthiophenyl)-4-ketobutanoyl-β-alanine 

Relevant academic research and scientific papers

Electrochemically generated organothiating reagents and their use

Electrolysis of organic disulfides in liquid sulfur dioxide is used to obtain organothiating agents, which can then be reacted with appropriate substrates to effect the synthesis of organothioaromatic compounds efficiently and in high yields. With appropriate phenolic compounds, regioselective substitution occurs in which para substitution greatly exceeds ortho substitution.

Electrochemical electrophilic aromatic methylthiation in liquid SO2

Controlled potential electrolysis of dimethyldisulfide in liquid sulfur dioxide provides a strongly electrophilic methylthiating agent. This species methylthiates strongly to weakly activated arenes in good to excellent yield.

A reductive acidolysis final deprotection strategy in solid phase peptide synthesis based on safety-catch protection

A reductive acidolysis final deprotection strategy in solid phase peptide synthesis was developed using a new safety-catch type of semi- permanent protecting groups and new linkers which were derived from 4- methylsulfinylbenzyl protection. This new strat

B12 Mimicry in a Weak Ligand Environment: Oxidation and Alkylation of Thiols

The first examples of alkylation and oxidation of thiols by cobalt in weakly coordinating ligand (MeCN) environments is presented as a mimic to B12-dependent nonenzymatic reaction.

A New Reductive Acidolysis Final Deprotection Strategy in Solid Phase Peptide Synthesis. Use of a New Safety-Catch Linker

A new reductive acidolysis final deprotection strategy in solid phase peptide synthesis was developed using a new safety-catch linker; this new strategy was based on a two-dimensional protection scheme employing acid-labile temporary and acid-stable but reductive acidolysiscleavable semipermanent protecting groups.