Quinolin-6-ylboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and boron-containing substances. This reagent contains a boronic acid group attached to a quinoline ring, which provides it with unique reactivity and versatility in synthetic chemistry. Its structural features enable it to participate in various reaction mechanisms, making it a valuable tool for chemists working in both academic and industrial settings. Due to its functional groups, it is often employed in coupling reactions that require boron-based reagents.
The compound is known for its chemical stability under controlled conditions, yet it exhibits high reactivity when exposed to elevated temperatures or catalytic influences. This dual nature makes it suitable for a range of synthetic applications where precise control over reaction conditions is essential. Its ability to form complexes with various ligands further enhances its utility in creating complex molecular structures. These properties make it a preferred choice for researchers aiming to achieve high selectivity and efficiency in their chemical processes.
In Indonesian laboratories, Quinolin-6-ylboronic Acid is commonly used in research settings such as universities, research institutions, and pharmaceutical companies. It plays a key role in the development of new drugs, industrial chemicals, and advanced materials. Its availability supports ongoing scientific innovation and contributes to the advancement of chemical research in the region.
TCI brochures (PDF)
- Boron Compounds 2025-10-07 · p. 14
Related TCI products
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- TCI T3325 182281-01-2 4-(Tetrahydro-2H-pyran-2-yloxy)phenylboronic Acid (contains varying amounts of Anhydride)
- TCI T2621 160032-40-6 Thieno[3,2-b]thiophene-2-boronic Acid (contains varying amounts of Anhydride)
- TCI T1975 6165-69-1 3-Thiopheneboronic Acid (contains varying amounts of Anhydride)
- TCI B5145 213318-44-6 1-(tert-Butoxycarbonyl)indole-2-boronic Acid (contains varying amounts of Anhydride)
- TCI B4774 113893-08-6 Benzo[b]thiophene-3-boronic Acid (contains varying amounts of Anhydride)
- Organic synthesis of heterocyclic compounds due to its boronic acid functionality and quinoline ring structure.
- Suzuki-Miyaura coupling reactions where boronic acid reagents are essential for forming carbon-carbon bonds.
- Heck reactions requiring boron-based reagents to facilitate cross-coupling between aryl halides and alkenes.
- Pharmaceutical research for the development of novel drug molecules involving boron-containing scaffolds.
- Material science applications in the synthesis of advanced polymers and functional materials with boron-based functionalities.
| Brand | TCI |
|---|---|
| CAS number | 376581-24-7 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | 24 g |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight. |
Quinolin-6-ylboronic Acid 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 exposure to moisture and air, which may affect its reactivity. The compound is sensitive to temperature changes and should be handled with care to avoid degradation. In laboratory settings, it is advisable to use appropriate personal protective equipment such as gloves and safety goggles when handling this material. Proper ventilation is also essential to ensure safe working conditions. Storage away from incompatible substances is crucial to prevent unwanted chemical interactions.
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