6-Indoleboronic Acid (TCI I0803) is a chemical compound widely used in laboratory settings for its unique reactivity in organometallic reactions. This reagent plays a crucial role in the synthesis of heterocyclic compounds and boron-containing molecules, making it an essential tool for chemists working in synthetic chemistry. Its structural features, including the presence of a boronic acid group, enable it to participate in various chemical transformations such as coupling reactions, reductions, and substitutions. Due to its versatility, it is frequently employed in research aimed at creating complex molecular structures.
One of the key properties that make 6-Indoleboronic Acid a preferred choice is its ability to form stable complexes with transition metals. This characteristic allows it to be used in the development of organometallic compounds, which are vital in both academic and industrial research. Additionally, its solubility in organic solvents enhances its usability across a wide range of chemical processes. The compound’s reactivity and compatibility with various reagents make it a reliable and efficient material for laboratory applications.
In Indonesian laboratories, 6-Indoleboronic Acid is extensively used in organic chemistry research, particularly in the fields of pharmacology, material science, and biochemical synthesis. Its relevance lies in its ability to facilitate the formation of complex structures that are essential for drug development and advanced material design. Researchers in Indonesia rely on this compound for its consistent performance and adaptability in different experimental conditions.
TCI brochures (PDF)
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 13
- Boron Compounds 2025-10-07 · p. 13
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 in coupling reactions and its ability to form stable boron-containing intermediates.
- Development of transition metal complexes for catalytic applications, leveraging its capacity to bind with metal ions and enhance reaction efficiency.
- Biochemical synthesis of complex molecules, as it supports the construction of structures involving boron and nitrogen atoms in biologically relevant contexts.
- Material science research for creating new boron-based materials with unique electronic and structural properties.
- Pharmaceutical research for the synthesis of drug molecules that require boronic acid functionalities for improved biological activity and stability.
| Brand | TCI |
|---|---|
| CAS number | 147621-18-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid or powder, depending on the specific product variant |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
6-Indoleboronic Acid should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture, which can affect its reactivity. The material should be stored away from incompatible substances such as strong oxidizers to ensure safety in the laboratory. Proper labeling of storage containers is essential for easy identification and safe handling. Regular inspection of storage conditions is advised to ensure optimal preservation of the compound. All handling should be performed with appropriate personal protective equipment to minimize exposure risks.
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