2,4,4,5,5-Pentamethyl-1,3,2-dioxaborolane is a versatile organoboron compound widely used in organic chemistry laboratories. As a key reagent in various synthetic processes, it plays a crucial role in facilitating complex molecular transformations. Its unique structure, featuring a boron center surrounded by multiple methyl groups, makes it highly reactive and suitable for a range of chemical reactions. This compound is particularly valuable in modern synthetic strategies due to its ability to participate in specific and controlled reactions, enhancing the efficiency of chemical synthesis.
The compound's reactivity stems from its boron-containing functional group, which is highly compatible with a variety of substrates. Its stability under specific conditions ensures consistent performance in laboratory settings, making it a reliable choice for researchers. Additionally, its ability to form stable intermediates contributes to its effectiveness in coupling reactions. These properties make it a preferred reagent for chemists aiming to achieve high-purity products in their synthetic pathways.
In Indonesian laboratories, 2,4,4,5,5-Pentamethyl-1,3,2-dioxaborolane is commonly used in organic synthesis research, especially in the development of pharmaceutical compounds and advanced materials. Its application is widespread in academic and industrial research settings, supporting the creation of complex molecules with specific functional groups. The compound's reliability and effectiveness make it an essential tool for chemical synthesis in both academic and applied research environments.
TCI brochures (PDF)
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 19
- Boron Compounds 2025-10-07 · p. 14
Related TCI products
- TCI T4407 1609484-75-4 4,4,5,5-Tetramethyl-2-(spiro[fluorene-9,9'-xanthen]-4-yl)-1,3,2-dioxaborolane
- TCI T4387 1160862-12-3 4,4,5,5-Tetramethyl-2-(spiro[fluorene-9,9'-xanthen]-2-yl)-1,3,2-dioxaborolane
- TCI T4061 870004-04-9 4,4,5,5-Tetramethyl-2-(4-vinylphenyl)-1,3,2-dioxaborolane
- TCI T3875 1080632-76-3 2-([1,1':4',1''-Terphenyl]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- TCI T3831 269410-26-6 4,4,5,5-Tetramethyl-2-(4-phenoxyphenyl)-1,3,2-dioxaborolane
- TCI T3710 171364-83-3 4,4,5,5-Tetramethyl-2-(4-nitrophenyl)-1,3,2-dioxaborolane
- Organic synthesis for creating complex molecular structures due to its reactivity and stability.
- Suzuki-Miyaura coupling reactions because of its compatibility with aromatic halides and its role in forming carbon-carbon bonds.
- Kumada-Corriu cross-coupling for its ability to facilitate reactions with organometallic reagents and alkyl halides.
- Pharmaceutical research for the development of new drug molecules with specific functional groups.
- Material science applications in the synthesis of advanced organic materials with tailored properties.
| Brand | TCI |
|---|---|
| CAS number | 94242-85-0 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents] |
| Pack sizes | Available in various quantities as per standard laboratory supply |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
This compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or inert plastic to prevent contamination and degradation. Due to its reactive nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid exposure to incompatible substances and ensure proper disposal following standard chemical waste protocols. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory applications.
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