2-Allyl-5,5-dimethyl-1,3,2-dioxaborinane is a versatile organoboron compound widely used in chemical synthesis, particularly in the development of complex molecular structures. This compound plays a crucial role in modern laboratory settings, where it supports advanced synthetic methodologies. Its unique chemical structure enables it to participate in a variety of reactions, making it an essential tool for researchers in organic chemistry and molecular synthesis. Due to its reactivity and functional versatility, it is frequently employed in the creation of aromatic and heterocyclic compounds.
The compound's stability is ensured through stabilization with phenothiazine, which prevents degradation caused by oxidation. This stabilization significantly extends the shelf life and maintains the compound’s reactivity over time. Its specific reactivity and controlled behavior make it a preferred choice for laboratories requiring reliable and consistent chemical performance. The combination of stability and reactivity allows for precise control in synthetic processes, ensuring reproducibility and efficiency in experimental outcomes.
In Indonesian laboratories, this compound is highly relevant for research in organic chemistry, especially in academic and research institutions focused on molecular synthesis. Its solid form facilitates ease of handling and storage, making it a practical choice for both small-scale and larger research projects. Its application in key synthetic reactions, such as the Suzuki-Miyaura reaction, further solidifies its importance in the chemical research landscape of Indonesia.
TCI brochures (PDF)
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 15
- Boron Compounds 2025-10-07 · p. 14
Related TCI products
- TCI F0531 346656-39-1 2-(2-Fluorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane
- TCI C2823 214360-47-1 2-(2-Cyanophenyl)-5,5-dimethyl-1,3,2-dioxaborinane
- TCI C2004 346656-42-6 2-(2-Chlorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane
- TCI E0667 346656-34-6 Ethyl 2-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)benzoate
- TCI B5960 331958-92-0 2-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (stabilized with Phenothiazine)
- TCI D6559 1047644-76-7 1,4-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
- Organoboron Chemistry: This compound is ideal for reactions requiring organoboron reagents, offering high reactivity and stability in complex synthetic pathways.
- Molecular Synthesis: Its ability to participate in selective transformations makes it a preferred choice for constructing complex organic molecules.
- Aromatic Compound Synthesis: The compound is widely used in the synthesis of aromatic and heterocyclic compounds due to its reactivity in cross-coupling reactions.
- Research and Development: Laboratories engaged in R&D benefit from its reliability and controlled reactivity, supporting innovative chemical processes.
- Academic Research: It is commonly used in universities and research institutions for teaching and experimental studies in organic chemistry.
| Brand | TCI |
|---|---|
| CAS number | 911482-75-2 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | Available in standard laboratory quantities as per supplier specifications |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and potential oxidation. Due to its stabilized nature with phenothiazine, it remains chemically inert under normal storage conditions. In a laboratory setting, it is important to handle the compound with care, using appropriate personal protective equipment to ensure safety. Proper labeling and storage practices will help maintain its quality and effectiveness for use in chemical synthesis. Always ensure that the compound is kept in a secure location, away from incompatible materials to prevent any unwanted reactions.
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