Quinoline-3-boronic Acid (TCI Q0080), with CAS number 191162-39-7, is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and boron-containing substances. This reagent plays a crucial role in modern synthetic chemistry due to its unique structural features, which include a quinoline ring linked to a boronic acid group. Its versatility makes it an essential component in various laboratory processes, especially in reactions requiring high precision and controlled environments.
The compound is known for its chemical stability under specific conditions, although it is highly sensitive to moisture and UV light. These properties make it ideal for applications where environmental control is paramount. The presence of an anhydride in the compound enhances its reactivity, allowing for more efficient and selective chemical transformations. This characteristic is particularly valuable in advanced synthetic protocols.
In Indonesian laboratories, Quinoline-3-boronic Acid is a key reagent for organic chemistry research, especially in academic and research institutions. Its availability supports the development of complex molecular structures and contributes to the advancement of chemical sciences in the region. Researchers benefit from its reliability and performance in demanding experimental settings.
TCI brochures (PDF)
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 14
- Boron Compounds 2025-10-07 · p. 13
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)
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- Suzuki Coupling Reactions: This reagent is ideal for Suzuki coupling due to its reactivity and compatibility with palladium catalysts, enabling efficient cross-coupling of aromatic compounds.
- Kumada Coupling Applications: It serves as a valuable organoboron reagent in Kumada coupling, facilitating the formation of carbon-carbon bonds under controlled reaction conditions.
- Heterocyclic Synthesis: Its quinoline structure makes it suitable for the synthesis of various heterocyclic compounds, which are essential in pharmaceutical and material sciences.
- Boron-Containing Compound Development: The compound is used in the creation of boron-based molecules, which have applications in medicinal chemistry and advanced materials.
- Precision Organic Synthesis: Its stability and reactivity make it suitable for experiments requiring high precision and controlled environmental conditions.
| Brand | TCI |
|---|---|
| CAS number | 191162-39-7 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | As per supplier specifications |
| Physical form | Solid (as per standard product description) |
| Storage | Requires dry, cool, and dark conditions to maintain stability and prevent degradation. |
Quinoline-3-boronic Acid should be stored in a dry, cool, and dark environment to prevent moisture-induced degradation and maintain its chemical integrity. It is recommended to use airtight containers made of glass or polyethylene to minimize exposure to humidity and UV light. Due to its sensitivity, the compound should be handled in a controlled laboratory setting with appropriate safety measures, such as gloves and a fume hood. Avoid prolonged exposure to light and ensure proper ventilation during use. Regular monitoring of storage conditions is essential to ensure the reagent remains effective for its intended applications.
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