2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI M3020

Chemical Identity

CAS No.: 610768-32-6
PubChem: CID 16414272·SID 468592247
Formula: C12H18BNO2
Molecular weight: 219.09 g/mol
Purity: >98.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-methyl-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)C
InChIKey: JEECGGXGHJUYMN-UHFFFAOYSA-N

Rp 1.749.300,00

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2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a specialized organoboron compound used in advanced chemical reactions, particularly in the field of organometallic chemistry. This reagent plays a crucial role in the synthesis of heterocyclic compounds and boron-containing molecules, making it an essential tool for researchers working on complex chemical structures. Its unique molecular structure, featuring a boronic acid group, allows it to participate in a variety of catalytic and coupling reactions, enhancing its versatility in synthetic applications.

The compound’s stability and reactivity make it a preferred choice for laboratory use. The presence of the boron group provides specific reactivity, enabling it to engage in reactions such as Suzuki-Miyaura coupling, which is widely used in organic synthesis. Its solubility in common organic solvents further simplifies its handling and application in laboratory settings. These properties ensure that it remains a reliable and efficient reagent for a wide range of chemical processes.

In Indonesian laboratories, this compound is widely utilized in organic chemistry research and the synthesis of complex molecules. Its availability in the local market makes it a go-to reagent for scientists and researchers working on pharmaceutical and material science projects. Its role in creating novel compounds with potential applications in various scientific fields underscores its importance in the Indonesian scientific community.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 19

Related TCI products

Organic Synthesis: This compound is ideal for creating complex organic molecules due to its reactivity and compatibility with various synthetic methods.
Suzuki-Miyaura Coupling Reactions: Its boronic acid functionality makes it a key reagent in this widely used coupling reaction for carbon-carbon bond formation.
Heterocyclic Compound Synthesis: The compound’s structure supports the formation of heterocyclic rings, which are essential in pharmaceutical and material science applications.
Material Science Research: It is used in the development of new materials, particularly those requiring boron-based functional groups for enhanced properties.
Pharmaceutical Development: Its role in synthesizing bioactive compounds makes it valuable in drug discovery and development projects.

Brand	TCI
CAS number	610768-32-6
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid or solid, depending on the specific formulation
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 chemical integrity. It is recommended to use airtight containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation and to follow standard safety protocols when working with organoboron compounds. Regular monitoring of storage conditions will help preserve the compound’s effectiveness and safety for use in chemical reactions.

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