PI13867 3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridazine (CAS No.: 1350543-95-1)

3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridazine Description

This compound, with the chemical formula C11H17BN2O2, serves as an intermediate in organic synthesis. The boronate ester functionality enables efficient transition-metal-catalysed cross-coupling reactions, which are vital in forming carbon–carbon bonds. Its off-white powder form ensures homogenous dispersion in reaction mixtures, promoting reproducible synthetic outcomes. Analytical assessments confirm that the compound maintains high purity, supporting its consistent performance in laboratory applications.

3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridazine Characteristics

*The above product information is based on theoretical data and is for reference only. Actual specifications may vary.

3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridazine Applications

Organic Synthesis
- Used as an intermediate in Suzuki coupling reactions to achieve efficient carbon–carbon bond formation by leveraging its boronate ester functionality.
- Applied as a reagent in multi-step synthesis routes to introduce pyridazine frameworks, enhancing molecular diversity through predictable reactivity.

Pharmaceutical Intermediate Development
- Serves as a building block in the synthesis of active pharmaceutical ingredients, enabling precise modification of molecular structures by exploiting its high purity and defined reactivity.
- Frequently used in reaction setups that require a consistent and reproducible reagent to optimise overall synthetic yields.

3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridazine Packing

The compound is packaged in airtight, moisture-resistant containers to prevent contamination and preserve chemical stability. It is sealed within secondary protective pouches and rigid outer boxes to safeguard against mechanical damage. Storage under controlled room temperature in a dry, dark environment is recommended. Options for customisation such as vacuum-sealed packaging and specific labelling are available upon request to meet laboratory handling requirements.

Additional Information

Boronate esters are integral components in modern synthetic organic chemistry due to their ability to participate in cross-coupling reactions. They enable the formation of complex molecular architectures through reliable transition-metal-catalysed processes. The reactivity profile of these compounds supports diverse applications ranging from academic research to industrial-scale synthesis.

Understanding the role of heterocyclic compounds like pyridazines enhances the ability to design targeted synthesis pathways. The controlled reactivity and structural specificity provided by such materials are critical in developing efficient synthesis protocols and advancing chemical research.