Indazole-4-boronic Acid (1023595-17-6) is a chemical compound widely used in organic laboratory settings. It serves as a versatile reagent in various synthetic processes, particularly in the formation of heterocyclic compounds and coupling reactions. This compound is a key component in modern synthetic chemistry due to its ability to participate in multiple reaction pathways. Its structural features, including the presence of a boronic acid group, make it highly reactive under specific conditions, enabling it to form stable intermediates with a variety of substrates. This reactivity is crucial in the development of complex molecules in both academic and industrial research environments.
The compound's unique chemical properties make it a preferred choice for chemists working in advanced synthesis. Its boronic acid functionality allows for efficient coupling reactions, such as the Suzuki-Miyaura and Kumada-Corriu reactions, which are essential in the synthesis of pharmaceuticals and materials. Additionally, the presence of anhydride impurities can influence its reactivity, making it important to consider during synthesis planning. These characteristics ensure that it remains a valuable tool in the hands of researchers aiming for controlled and reproducible chemical transformations.
In Indonesian laboratories, Indazole-4-boronic Acid is commonly used in organic chemistry research, especially in the development of pharmaceutical compounds and inorganic materials. Its ability to react under controlled conditions makes it a go-to reagent for scientists working on complex molecular structures. Researchers in educational and research institutions frequently rely on this compound for its reliability and effectiveness in various synthetic applications.
TCI brochures (PDF)
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 14
Related TCI products
- TCI T3706 108847-76-3 1-Thianthrenylboronic Acid (contains varying amounts of Anhydride)
- 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 reactivity and coupling capabilities.
- Use in Suzuki-Miyaura cross-coupling reactions for efficient carbon-carbon bond formation.
- Application in Kumada-Corriu coupling for the synthesis of complex organic molecules.
- Research in pharmaceutical development for the creation of novel drug compounds.
- Investigation of inorganic material synthesis through controlled chemical reactions.
| Brand | TCI |
|---|---|
| CAS number | 1023595-17-6 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | As listed on product page |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
Indazole-4-boronic Acid should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air, which can affect its reactivity. Due to its potential reactivity with heavy metals and oxidizing agents, it should be handled with care, using appropriate personal protective equipment. Storage away from incompatible substances is essential to ensure safety in the laboratory. Regular monitoring of storage conditions is advised to maintain the integrity of the compound during long-term use. Proper labeling and containment are necessary to prevent accidental exposure and ensure safe handling practices.
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