2-Methylthiophene is a chemical compound classified under the heterocyclic category, commonly used as a foundational building block in the synthesis of complex compounds. Its unique molecular structure features a sulfur atom and a carbon atom arranged within a heterocyclic ring, making it a versatile reagent in organic chemistry. In laboratory settings, this compound plays a crucial role in constructing organic molecules with specific biological or chemical properties. Its reactivity is particularly notable due to the presence of the sulfur atom and the heterocyclic ring, which can participate in various chemical reactions.
The chemical properties of 2-Methylthiophene make it a preferred choice for laboratory applications. It exhibits high reactivity, especially with reagents such as acids, bases, and alkali metals, enabling it to undergo substitution, oxidation, and reduction reactions. Its solubility in organic solvents further enhances its utility in laboratory procedures, facilitating mixing and separation processes. These characteristics make it an essential component in synthetic pathways that require structural modifications of organic molecules.
In Indonesian laboratories, 2-Methylthiophene is widely used in chemical research, particularly in the synthesis of organic compounds and the study of molecular structures. Its availability and reactivity make it a valuable tool for researchers working on drug development, material science, and other chemical disciplines. The compound’s role in creating complex organic structures supports a wide range of scientific investigations in both academic and industrial settings.
TCI brochures (PDF)
- Thiophenes 2026-06-29 · p. 2
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- Organic synthesis: 2-Methylthiophene is ideal for creating complex organic molecules due to its reactivity and structural versatility.
- Drug development: It is used in the synthesis of pharmaceutical compounds, as its heterocyclic structure can mimic biological molecules.
- Material science research: The compound’s chemical properties make it suitable for developing new materials with specific functional characteristics.
- Analytical chemistry: It serves as a reference standard for identifying and quantifying thiophene derivatives in various samples.
- Environmental studies: Its reactivity and solubility make it useful in studying the behavior of sulfur-containing compounds in different environments.
| Brand | TCI |
|---|---|
| CAS number | 554-14-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Heterocyclic Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from light and incompatible materials |
2-Methylthiophene should be stored in a cool, dry environment, away from direct light and incompatible substances such as strong oxidizing agents. It is recommended to use sealed, airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it should be stored in a well-ventilated area to minimize exposure. Always ensure that the storage area is secure and inaccessible to unauthorized personnel. Proper labeling and documentation are essential for safe handling and regulatory compliance.
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