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4-[(1-Pyrrolidinyl)carbonyl]phenylboronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of complex molecules involving boron-based reactions. This reagent plays a crucial role in the formation of new bonds through specific reaction mechanisms, making it an essential tool in modern chemical laboratories. Its unique molecular structure, featuring a reactive boronic acid group, allows it to participate in various coupling reactions. This versatility makes it a valuable component in the development of new compounds with tailored properties.
The compound's reactivity and ability to form stable intermediates make it a preferred choice for chemists working on precise and controlled chemical processes. Its capacity to interact with a wide range of organic substrates enhances its utility in synthetic pathways. The presence of the pyrrolidinyl group further increases its functional versatility, enabling it to be used in multiple reaction types. These properties contribute to its popularity in both academic and industrial research settings.
In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmaceutical, material science, and environmental chemistry applications. It is frequently employed in experiments requiring high precision and controlled reaction conditions. Its role in synthesizing complex organic structures makes it a key reagent in both teaching and research environments across various scientific disciplines.
TCI brochures (PDF)
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 7
- Boron Compounds 2025-10-07 · p. 9
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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- Organic Synthesis: This compound is ideal for synthesizing complex organic molecules due to its reactivity and ability to form stable intermediates in coupling reactions.
- Pharmaceutical Research: It is widely used in drug development for creating novel compounds with specific biological activities and structural properties.
- Material Science: The compound's unique structure enables it to be used in the development of advanced materials with tailored chemical and physical properties.
- Environmental Chemistry: It plays a role in the synthesis of compounds used for environmental monitoring and remediation processes.
- Teaching and Research: It is a common reagent in academic settings for demonstrating and conducting advanced organic reactions and synthetic pathways.
| Brand | TCI |
|---|---|
| CAS number | 389621-81-2 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | As listed on product packaging |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
This compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. Due to its reactive nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Storage should be in a well-ventilated area to minimize the risk of inhalation of any vapors. Avoid contact with incompatible materials to ensure safe handling and long-term stability. Always follow standard laboratory safety protocols when working with this reagent.
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