5-Pyrimidylboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of complex boron-containing compounds. This reagent plays a crucial role in laboratory settings where precision and efficiency in chemical reactions are essential. Its unique structure allows it to participate in various coupling reactions, making it a valuable tool for chemists and researchers. In Indonesia, this compound is frequently utilized in academic and industrial laboratories for the development of new chemical entities and advanced materials.
The compound is preferred due to its ability to form complexes with transition metals, enhancing the efficiency and specificity of chemical reactions. Its stability under certain conditions ensures safe handling and reliable performance in laboratory experiments. Additionally, its reactivity and selectivity make it ideal for applications requiring high precision. These properties make it a go-to reagent for researchers working on complex molecular structures and pharmaceutical compounds.
In Indonesian laboratories, 5-Pyrimidylboronic Acid is commonly used in both research and educational settings. It supports the development of new drugs and materials, contributing to advancements in pharmacology and chemical engineering. Its relevance extends to academic institutions, where it is used to teach and demonstrate key concepts in organic chemistry and synthetic methodologies.
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 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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- Organic Synthesis: This compound is ideal for synthesizing complex organic molecules, especially those involving boron.
- Suzuki Coupling Reactions: It is a key reagent in Suzuki reactions, enabling efficient cross-coupling of aryl halides with boronic acids.
- Heck Reactions: It supports the formation of carbon-carbon bonds in Heck reactions, which are critical in pharmaceutical synthesis.
- Pharmaceutical Development: Its role in creating boron-containing compounds makes it valuable in drug discovery and development.
- Educational Research: It is widely used in academic settings to teach and research advanced organic chemistry techniques.
| Brand | TCI |
|---|---|
| CAS number | 109299-78-7 |
| 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 | Store in a cool, dry place away from moisture and direct sunlight |
5-Pyrimidylboronic Acid should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid exposure to moisture and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize any potential risks associated with its chemical properties. Proper labeling and storage conditions ensure safe handling and long-term usability in laboratory settings.
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