7-Bromoquinoline is a chemical compound belonging to the heterocyclic category, characterized by a quinoline core with a bromine substituent at the 7-position. This compound plays a significant role in laboratory settings, particularly in organic chemistry and pharmacology, where it serves as a key building block for the synthesis of complex molecules. Its structural stability and reactivity make it a valuable resource for researchers aiming to develop new compounds with biological activity.
The unique properties of 7-Bromoquinoline, including its strong aromatic character and reactivity in electrophilic reactions, make it a preferred choice in various chemical processes. It is especially useful in substitution reactions, ring-opening reactions, and reactions involving nucleophiles. Its ability to participate in halogen substitution, hydroxylation, and other functional group transformations enhances its versatility in synthetic applications.
In Indonesian laboratories, 7-Bromoquinoline is commonly used in scientific research, particularly in the fields of organic chemistry and pharmaceutical development. It is an essential component in the synthesis of bioactive compounds, contributing to the advancement of drug discovery and chemical innovation. Its widespread application in both academic and industrial research underscores its importance in modern chemical studies.
TCI brochures (PDF)
- Aryne/Heteroaryne Precursors 2025-09-16 · p. 8
- Organic synthesis applications benefit from 7-Bromoquinoline due to its reactivity and structural versatility, enabling the creation of complex molecules.
- Pharmaceutical research utilizes this compound for the development of bioactive agents, leveraging its ability to participate in various chemical transformations.
- Heterocyclic compound synthesis relies on 7-Bromoquinoline as a core structure, allowing for the modification of functional groups to achieve desired biological properties.
- Industrial chemical production incorporates this compound in the manufacturing of specialty chemicals, thanks to its stability and reactivity.
- Academic research in chemistry and pharmacology frequently employs 7-Bromoquinoline to explore new synthetic pathways and molecular structures.
| Brand | TCI |
|---|---|
| CAS number | 4965-36-0 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Heterocyclic Building Blocks |
| Pack sizes | — |
| Physical form | — |
| Storage | Store in a cool, dry place away from light and incompatible materials |
7-Bromoquinoline should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn. Avoid contact with incompatible substances like strong oxidizing agents. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications. Proper labeling and storage practices help maintain the integrity of the material and ensure safe handling in a laboratory setting.
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