3'-Aminoacetanilide is a chemical compound widely utilized in synthetic chemistry, particularly in organic research. It serves as a versatile building block in the development of various compounds, including pharmaceuticals, industrial chemicals, and functional intermediates. This compound is derived from acetanilide with an amino group substituted at the 3-position, which enhances its reactivity and functional versatility. Its unique structure allows it to participate in multiple chemical reactions, making it an essential reagent in laboratory settings.
The chemical properties of 3'-Aminoacetanilide make it a preferred choice for chemists. It exhibits moderate stability while maintaining sufficient reactivity to engage in reactions such as hydrolysis, nitration, and electrophilic substitution. Its molecular structure also facilitates its use in studying reaction mechanisms, offering valuable insights into chemical behavior. These characteristics contribute to its popularity among researchers seeking reliable and adaptable reagents.
In Indonesian laboratories, 3'-Aminoacetanilide is commonly used in organic chemistry research. It is a key component in experiments requiring specific structural intermediates. Institutions such as universities and research centers rely on this compound for synthetic processes and analytical studies. Its availability in solid form and ease of handling make it a practical choice for both academic and industrial applications.
- Organic synthesis experiments benefit from 3'-Aminoacetanilide due to its reactivity and structural versatility, enabling the creation of complex molecules.
- Pharmaceutical research utilizes this compound as a building block for drug development, offering a foundation for synthesizing active pharmaceutical ingredients.
- Industrial chemical production incorporates 3'-Aminoacetanilide in the manufacture of specialty chemicals, leveraging its functional groups for targeted modifications.
- Analytical chemistry applications use it as a standard for identifying and quantifying similar compounds through various analytical techniques.
- Teaching laboratories employ this compound to demonstrate fundamental chemical reactions and synthetic pathways to students.
| Brand | TCI |
|---|---|
| CAS number | 102-28-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from direct sunlight |
3'-Aminoacetanilide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to strong oxidizing agents or incompatible substances. Proper ventilation is essential when working with this compound to ensure a safe laboratory environment. Regular inspection of storage conditions is advised to ensure long-term integrity and usability.
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