2-Iodoterephthalic Acid is a chemical compound widely used in laboratory settings, particularly in organic synthesis reactions. It serves as a key reagent in the development of complex organic molecules, playing a crucial role in various chemical processes. Due to its unique molecular structure, which includes two carboxylic acid groups and one iodide group, it is highly reactive and versatile in chemical applications. This compound is especially valuable in nucleophilic substitution and coupling reactions, where its iodide functionality acts as a reactive site.
The compound's reactivity and stability make it a preferred choice for researchers working in synthetic chemistry. Its ability to participate in reactions requiring iodide as a reagent or catalyst is a significant advantage. The clear physical and chemical properties of 2-Iodoterephthalic Acid ensure consistency and reliability in experimental outcomes. Additionally, its ease of handling and processing further enhance its appeal in laboratory environments.
In Indonesian laboratories, 2-Iodoterephthalic Acid is commonly used in organic chemistry research, especially in the synthesis of complex compounds and the study of aromatic reactivity. It is a staple in academic and research institutions, supporting studies in pharmaceuticals, materials science, and analytical chemistry. Its availability and performance make it a trusted material for scientific investigations.
TCI brochures (PDF)
- Iodinated Phenol／Benzoic Acid／Benzaldehyde Building Blocks 2024-11-15 · p. 2
- Organic synthesis of complex compounds where iodide functionality is essential for reaction mechanisms.
- Development of pharmaceutical intermediates requiring precise chemical transformations and reactivity.
- Research in materials science for the creation of functional polymers and advanced chemical structures.
- Analytical chemistry applications involving iodide-based reagents for detection and quantification.
- Study of aromatic reactivity in chemical reactions, particularly in substitution and coupling processes.
| Brand | TCI |
|---|---|
| CAS number | 1829-22-7 |
| Molecular formula | — |
| Purity | — |
| Category | TCI |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
2-Iodoterephthalic Acid should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture, which can affect its stability. Due to its reactivity, it should be handled with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances and ensure proper ventilation in the workspace. The compound is generally stable under standard laboratory conditions, making it suitable for routine use in chemical synthesis and research applications. Always follow standard laboratory safety protocols when working with this material.
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