Thiophen-2-ol
97%
- Product Code: 244182
CAS:
17236-58-7
| Molecular Weight: | 100.14 g./mol | Molecular Formula: | C₄H₄OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01075765 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, light-proof, inert gas |
Product Description:
Thiophen-2-ol is primarily used as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its sulfur-containing aromatic structure makes it valuable in constructing complex molecules where heterocyclic frameworks are needed. It participates in coupling reactions, such as Suzuki and Ullmann reactions, enabling the formation of biaryl systems used in drug development.
It is also employed in the synthesis of functional materials, including conductive polymers and organic semiconductors, due to the electron-rich nature of the thiophene ring. Derivatives of thiophen-2-ol can act as ligands in catalytic metal complexes, enhancing reaction efficiency in industrial processes.
Additionally, it finds use in the preparation of dyes, sensors, and specialty chemicals where aromatic sulfur compounds contribute to desired optical or electronic properties. Its reactivity allows for easy modification, making it a versatile building block in both research and industrial applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €285.41 |
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| 0.250 | 10-20 days | €428.12 |
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Thiophen-2-ol
Thiophen-2-ol is primarily used as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its sulfur-containing aromatic structure makes it valuable in constructing complex molecules where heterocyclic frameworks are needed. It participates in coupling reactions, such as Suzuki and Ullmann reactions, enabling the formation of biaryl systems used in drug development.
It is also employed in the synthesis of functional materials, including conductive polymers and organic semiconductors, due to the electron-rich nature of the thiophene ring. Derivatives of thiophen-2-ol can act as ligands in catalytic metal complexes, enhancing reaction efficiency in industrial processes.
Additionally, it finds use in the preparation of dyes, sensors, and specialty chemicals where aromatic sulfur compounds contribute to desired optical or electronic properties. Its reactivity allows for easy modification, making it a versatile building block in both research and industrial applications.
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