5-Formyl-2-thiophenecarboxylic Acid is a versatile organic compound widely used in laboratory settings for its reactivity and structural adaptability. It belongs to the class of heterocyclic building blocks, featuring a thiophene ring with a formyl group at the 5-position. This compound plays a crucial role in synthetic chemistry, serving as a foundational element for the development of complex molecules. Its unique structure allows it to participate in various chemical reactions, making it an essential tool for researchers in multiple scientific disciplines.
The compound’s reactivity is primarily attributed to its formyl group and thiophene ring, which are highly susceptible to chemical modifications. These functional groups enable it to react with a wide range of reagents, including amines, alcohols, and other active functional groups. This versatility makes it a preferred choice for chemists seeking to synthesize compounds with tailored properties. Its ability to undergo condensation, substitution, and catalytic reactions further enhances its value in synthetic processes.
In Indonesian laboratories, 5-Formyl-2-thiophenecarboxylic Acid is commonly used in pharmaceutical and organic chemistry research. Researchers utilize it to develop new compounds with potential applications in drug discovery and material science. Its availability and chemical properties make it a reliable and widely used building block in both academic and industrial research environments.
TCI brochures (PDF)
- Thiophenes 2026-06-29 · p. 10
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- Organic synthesis: This compound is ideal for creating complex molecules due to its reactive thiophene ring and formyl group, enabling diverse chemical transformations.
- Pharmaceutical research: Its structural versatility allows it to be used in the development of new drugs and therapeutic agents, supporting medicinal chemistry efforts.
- Material science: The compound’s reactivity and functional groups make it suitable for synthesizing advanced materials with specific chemical properties.
- Catalytic reactions: Its ability to participate in catalytic processes makes it valuable in developing efficient and selective chemical reactions.
- Functional group modification: The formyl group and thiophene ring provide multiple sites for chemical modification, supporting the design of new compounds with tailored properties.
| Brand | TCI |
|---|---|
| CAS number | 4565-31-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Heterocyclic Building Blocks |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances, and ensure proper ventilation in the laboratory. Regular monitoring of storage conditions is advised to ensure the compound remains stable and usable for research purposes.
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