2,6-Dimethylbenzenethiol CAS 118-72-9: A Key Aromatic Thiol for Flavor, Fragrance, and Chemical Synthesis

Explore the versatile applications of 2,6-dimethylbenzenethiol in flavor, fragrance, and advanced chemical synthesis.

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Key Advantages

Reactive Thiol Group

The reactive thiol (–SH) group in 2,6-dimethylbenzenethiol allows for diverse chemical transformations, making it an excellent building block for introducing sulfur into organic molecules. This characteristic is invaluable for custom synthesis requirements.

Steric and Electronic Influence

The ortho methyl groups on the benzene ring provide steric hindrance and influence the electronic properties, offering enhanced selectivity in chemical reactions and contributing to the performance of ligands in catalysis.

Versatile Ligand Properties

As a soft sulfur donor, 2,6-dimethylbenzenethiol forms stable complexes with transition metals, crucial for applications in catalysis, analytical chemistry, and metal recovery processes.

Key Applications

Flavor & Fragrance Intermediates

Used as a key intermediate in the creation of specific flavor and fragrance profiles, contributing unique notes to various products.

Organic Synthesis

Serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty organic compounds, leveraging its reactive functional groups.

Coordination Chemistry

Functions as an effective ligand for transition metals, facilitating the development of catalysts and materials with specific properties.

Polymer and Rubber Industry

Can be employed as a vulcanization agent or modifier in rubber processing and as an intermediate for polymer stabilizers, enhancing material performance.

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