2-Amino-2',5-dichlorobenzophenone is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a key building block for the synthesis of complex molecules, particularly in the development of aromatic and heterocyclic compounds. This compound plays a crucial role in various synthetic pathways, including electrophilic substitution and condensation reactions. Its unique structure enables it to participate in multiple chemical transformations, making it a versatile reagent in organic chemistry.
The compound's reactivity is enhanced by the presence of an amino group and two chloro substituents, which contribute to its chemical versatility. These functional groups allow it to engage in a wide range of chemical interactions, making it a preferred choice for researchers. Its stability under controlled conditions further supports its use in laboratory applications. The combination of reactivity and stability ensures that it remains a valuable tool in both academic and industrial research environments.
In Indonesian laboratories, 2-Amino-2',5-dichlorobenzophenone is commonly used in organic chemistry, pharmaceutical, and materials science research. It is particularly favored for its ability to facilitate the synthesis of bioactive compounds and functional materials. Its availability and reliability make it a go-to reagent for scientists working on innovative chemical projects. Its role in advancing research in these fields continues to be significant.
- Organic synthesis of aromatic and heterocyclic compounds due to its reactive functional groups and structural versatility.
- Development of bioactive molecules in pharmaceutical research because of its ability to participate in diverse chemical transformations.
- Synthesis of functional materials in materials science due to its stable molecular structure and reactivity.
- Electrophilic substitution reactions as a key building block in the formation of complex organic molecules.
- Condensation reactions in the preparation of various organic compounds through its reactive amino and chloro groups.
| Brand | TCI |
|---|---|
| CAS number | 2958-36-3 |
| 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 light and moisture |
This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. Due to its reactive nature, it should be handled with care in a well-ventilated laboratory environment. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Avoid contact with incompatible substances to ensure safe storage and usage. Always follow standard laboratory safety protocols when working with this chemical.
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