Thiophen-2-ol

97%

Reagent Code: #244182
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CAS Number 17236-58-7

science Other reagents with same CAS 17236-58-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 100.14 g/mol
Formula C₄H₄OS
badge Registry Numbers
MDL Number MFCD01075765
inventory_2 Storage & Handling
Storage 2-8°C, dry, light-proof, inert gas

description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,800.00
inventory 250mg
10-20 days ฿16,200.00
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Thiophen-2-ol
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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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