6-(Morpholino)pyridine-3-boronic Acid is a chemical compound widely used in organic reactions, especially in the synthesis of heterocyclic compounds and boron-containing molecules. Its complex structure enables high reactivity under various chemical conditions, making it a valuable tool in synthetic chemistry. This compound is commonly employed as a reagent in coupling reactions, such as the Suzuki-Miyaura reaction, which is essential for the synthesis of complex molecules. Its reactivity is particularly notable towards transition metals and other organic compounds, enhancing its utility in diverse chemical processes.
The presence of varying amounts of anhydride in this compound provides flexibility in chemical reactions, allowing for a range of synthetic pathways. Its unique molecular structure enables the formation of complex bonds, making it a preferred choice for researchers seeking versatile reagents. The compound’s ability to participate in multiple reaction types and its compatibility with various reaction conditions contribute to its popularity in both academic and industrial settings.
In Indonesian laboratories, this compound is extensively used in organic chemistry research, particularly in higher education institutions and research organizations. Its availability, reliability, and effectiveness in a wide array of chemical reactions make it a top choice for local researchers. The compound plays a crucial role in advancing chemical synthesis and innovation within the scientific community in Indonesia.
TCI brochures (PDF)
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 14
- 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)
- Suzuki-Miyaura Coupling Reactions: This compound is ideal for coupling reactions due to its reactivity with transition metals and its ability to form complex molecular structures.
- Organic Synthesis of Heterocyclic Compounds: Its unique molecular structure allows it to participate in the synthesis of various heterocyclic compounds, enhancing the diversity of chemical products.
- Boron-Containing Molecule Synthesis: The compound is well-suited for the creation of boron-based molecules, which are essential in pharmaceutical and materials science research.
- Transition Metal Catalyzed Reactions: Its reactivity with transition metals makes it a suitable reagent for catalytic processes in synthetic chemistry.
- Complex Bond Formation in Organic Chemistry: Its ability to form new and complex bonds makes it a valuable tool in the development of advanced chemical structures.
| Brand | TCI |
|---|---|
| CAS number | 904326-93-8 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | — |
| Physical form | — |
| Storage | Store in a cool, dry place away from moisture and light |
This compound should be stored in a cool, dry place, away from moisture and direct light to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its chemical properties. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation should be maintained in the laboratory to minimize inhalation risks. The compound should not be stored near incompatible substances to avoid potential chemical interactions. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory applications.
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