2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI M2650

Chemical Identity

CAS No.: 445264-61-9
PubChem: CID 16217714·SID 253662296
Formula: C12H18BNO3
Molecular weight: 235.09 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CN=C(C=C2)OC
InChIKey: QOGNDJLSYMJGPP-UHFFFAOYSA-N

Rp 1.193.850,00

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2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a specialized organic compound used in advanced chemical research and synthesis. It plays a crucial role in laboratories where complex molecular structures are being developed, particularly in the field of organoboron chemistry. This compound is widely utilized in synthetic pathways that require precise reactivity and functional group compatibility. Its unique structure allows it to participate in various reaction mechanisms, making it a versatile tool for chemists working on heterocyclic and boron-containing compounds.

The compound's chemical properties make it a preferred choice for synthetic chemists. It exhibits stability under controlled conditions, which is essential for maintaining reaction efficiency. Its boron-containing group enables it to form stable intermediates in coupling reactions, such as Suzuki and Stille reactions. Additionally, its reactivity in S(N)1 and S(N)2 mechanisms allows for the synthesis of a wide range of organic compounds. These characteristics make it an essential component in modern synthetic strategies.

In Indonesian laboratories, this compound is commonly used by researchers, students, and pharmaceutical industries for the development of new chemical entities. Its application spans across academic and industrial settings, where it supports the creation of complex molecules. Due to its chemical versatility and reactivity, it is a key reagent in the synthesis of pharmaceuticals and other advanced materials. Its use is particularly prevalent in research focused on heterocyclic compounds and boron-based chemistry.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 17
Boron Compounds 2025-10-07 · p. 19

Related TCI products

Organic synthesis applications benefit from this compound's ability to participate in coupling reactions, enabling the formation of complex molecular structures with high efficiency.
Heterocyclic compound development relies on its reactivity in S(N)1 and S(N)2 mechanisms, allowing for the synthesis of diverse functional groups.
Pharmaceutical research utilizes its boron-containing group to create stable intermediates in drug molecule synthesis, enhancing reaction specificity.
Academic research in chemistry leverages its versatility for teaching and experimental purposes, supporting both undergraduate and graduate studies.
Industrial chemical production incorporates this compound for the development of advanced materials and specialty chemicals requiring precise synthetic pathways.

Brand	TCI
CAS number	445264-61-9
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various quantities to suit different laboratory needs
Physical form	Solid or liquid, depending on the specific formulation
Storage	—

This compound should be stored in a cool, dry place away from moisture and oxidizing agents to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent exposure to air and humidity. Due to its sensitivity to moisture, it is important to handle it in a controlled environment, ideally under an inert atmosphere such as nitrogen. Proper labeling and storage conditions are essential to ensure safety and maintain the compound's effectiveness. Laboratory personnel should wear appropriate personal protective equipment when handling this material to minimize any potential risks.

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