Ethyl 3,5-Dichloro-4-hydroxybenzoate is a chemical compound widely used in organic synthesis reactions within laboratory settings. This compound serves as a key building block for the development of various organic molecules, particularly in pharmaceutical and chemical research. Its molecular structure includes hydroxyl and chlorine groups at specific positions on the benzene ring, making it a versatile reagent for functional group transformations. Due to its stability and controlled reactivity, it is a reliable choice for chemists seeking to synthesize complex compounds with predictable outcomes.
The compound exhibits favorable chemical properties that make it a preferred choice in laboratory applications. It is soluble in organic solvents and can participate in substitution and esterification reactions, which are essential in synthetic pathways. These characteristics allow it to be used in a variety of experimental conditions, including those requiring moderate reactivity and molecular stability. Additionally, its non-heterocyclic nature simplifies purification and identification processes, making it a practical option for analytical chemistry.
In Indonesian laboratories, Ethyl 3,5-Dichloro-4-hydroxybenzoate is commonly used in scientific research and educational settings. It is a staple in organic chemistry experiments, particularly in the synthesis of pharmaceutical intermediates and other complex molecules. Many research institutions and universities rely on this compound for both teaching and experimental purposes, supporting the advancement of chemical knowledge in the region.
- Organic synthesis is a primary application where this compound serves as a versatile building block for creating complex molecules.
- Pharmaceutical research benefits from its use in the development of drug intermediates and active pharmaceutical ingredients.
- Analytical chemistry utilizes its non-heterocyclic structure for easier purification and identification in chemical analysis.
- Educational institutions employ it in teaching organic chemistry to demonstrate functional group transformations and reaction mechanisms.
- Industrial chemical processes incorporate it for the production of specialty chemicals and fine chemicals with specific properties.
| Brand | TCI |
|---|---|
| CAS number | 17302-82-8 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid powder |
| Storage | Store in a cool, dry place away from light and moisture |
Ethyl 3,5-Dichloro-4-hydroxybenzoate should be stored in a cool, dry place 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, which may affect its stability. Due to its chemical nature, it should be handled with appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory to minimize inhalation risks. The compound is not classified as hazardous under standard laboratory conditions, but standard safety protocols should still be followed when working with chemical reagents. Always follow established laboratory safety procedures to ensure safe handling and storage.
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