AB60703
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $15.00 | $10.00 | - + | |
1g | 97% | in stock | $16.00 | $11.00 | - + | |
5g | 97% | in stock | $19.00 | $14.00 | - + | |
10g | 97% | in stock | $37.00 | $26.00 | - + | |
25g | 97% | in stock | $69.00 | $49.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB60703 |
Chemical Name: | 2,6-Dimethylthiophenol |
CAS Number: | 118-72-9 |
Molecular Formula: | C8H10S |
Molecular Weight: | 138.23 |
MDL Number: | MFCD00010021 |
SMILES: | Cc1cccc(c1S)C |
2,6-Dimethylthiophenol, also known as dimethylthiolophenol, is a versatile compound widely utilized in chemical synthesis. Its unique properties make it a valuable reagent in various organic reactions and processes. In particular, 2,6-Dimethylthiophenol is commonly employed as a thiol building block in the preparation of sulfur-containing compounds.One of the key applications of 2,6-Dimethylthiophenol is its use as a thiolating agent in the modification of organic molecules. By reacting with various electrophiles, this compound introduces thiol groups into the target molecules, enabling the synthesis of thioethers, thioesters, and other sulfur-containing structures. This thiolation capability is essential in the development of pharmaceuticals, agrochemicals, and materials with specific functionalities.Furthermore, 2,6-Dimethylthiophenol serves as a valuable precursor in the synthesis of complex organic compounds. Its ability to participate in both nucleophilic aromatic substitution and cross-coupling reactions expands its utility in building molecular frameworks with sulfur linkages. This compound plays a crucial role in the construction of heterocyclic compounds and organosulfur polymers, contributing to the advancement of diverse fields in organic chemistry.In summary, the strategic incorporation of 2,6-Dimethylthiophenol in chemical synthesis offers a pathway to access sulfur-containing compounds with tailored properties and functionalities. Its reactivity and versatility make it an indispensable tool for organic chemists seeking to design and prepare novel molecules for various applications in research and industry.