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AB62381

1073-29-6 | 2-Hydroxythioanisole

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $25.00 $17.00 -   +
5g 98% in stock $38.00 $26.00 -   +
25g 98% in stock $88.00 $62.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB62381
Chemical Name: 2-Hydroxythioanisole
CAS Number: 1073-29-6
Molecular Formula: C7H8OS
Molecular Weight: 140.20282
MDL Number: MFCD00002211
SMILES: CSc1ccccc1O
NSC Number: 75839

 

Computed Properties
Complexity: 85  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • 2-(Methylthio)phenol, also known as 2-methylthiophenol, is a versatile compound that finds wide application in chemical synthesis. Its unique structure, featuring a thiol group attached to a phenyl ring, imparts several key properties that make it valuable in various processes.One prominent use of 2-(Methylthio)phenol is as a starting material in the synthesis of pharmaceuticals and agrochemicals. The thiol group can undergo a range of chemical reactions, including nucleophilic substitution and oxidation, allowing for the introduction of different functional groups. This versatility makes it a valuable building block in the creation of complex organic molecules with specific biological activities.In addition to its role in the synthesis of bioactive compounds, 2-(Methylthio)phenol is also utilized in the preparation of specialty chemicals and materials. Its sulfur-containing moiety can act as a chelating agent, forming coordination complexes with metal ions. This property is exploited in the development of catalysts for organic transformations and in the production of dyes and pigments.Furthermore, the presence of the aromatic phenyl ring in 2-(Methylthio)phenol allows for its incorporation into aromatic systems, enhancing the electronic properties of the resulting molecules. This is particularly important in materials science applications, where the tailored introduction of functional groups can modulate the properties of polymers and electronic materials.Overall, 2-(Methylthio)phenol serves as a valuable tool in the hands of chemists and researchers, enabling the creation of diverse compounds with tailored properties for applications spanning pharmaceuticals, agrochemicals, materials science, and beyond.
Literature
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