3-Amino-2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI A2993

Chemical Identity

CAS No.: 893440-50-1
PubChem: CID 59557920·SID 354333723
Formula: C12H19BN2O3
Molecular weight: 250.10 g/mol
Purity: >98.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-amine
SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC(=C(N=C2)OC)N
InChIKey: KYYKGOURQXPERA-UHFFFAOYSA-N

Rp 795.900,00

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Berat 200mg 1g

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3-Amino-2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a complex organic compound widely used in laboratory settings for its role in organometallic reactions and the synthesis of complex molecules. This reagent is particularly valuable in the field of chemical research due to its unique molecular structure, which includes a boron-containing group. This group enables the compound to participate in various coupling reactions, such as the Suzuki-Miyaura reaction, which is essential for the synthesis of heterocyclic compounds and pharmaceuticals. Its presence in the chemical toolbox of Indonesian laboratories highlights its importance in both academic and industrial research.

The compound’s reactivity stems from its boron-based functional group, which allows for selective and efficient bonding with a variety of ligands. This makes it a preferred choice for chemists working on synthetic pathways that require high specificity and yield. Additionally, its solubility in polar solvents enhances its utility in a wide range of chemical environments, making it adaptable to different experimental conditions. These properties make it a reliable and versatile reagent in modern chemical synthesis.

In Indonesian laboratories, this compound is commonly used in organic chemistry and pharmaceutical research. Its availability in international markets ensures that it is accessible to researchers in various institutions. Its application in the synthesis of complex molecules underscores its relevance in both academic and industrial research settings. Its role in coupling reactions further supports its importance in the development of new compounds and drug discovery efforts.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 18
Boron Compounds 2025-10-07 · p. 18

Related TCI products

Used in Suzuki-Miyaura coupling reactions for efficient cross-coupling of aryl halides with boronic acids, enabling the synthesis of complex heterocyclic compounds.
Applied in pharmaceutical research for the development of new drugs, particularly in the synthesis of bioactive molecules with specific functional groups.
Utilized in organic synthesis to introduce boronic acid functionalities into aromatic rings, enhancing the reactivity and selectivity of target molecules.
Employed in academic research for teaching and experimentation, providing students with hands-on experience in advanced synthetic techniques.
Integrated into industrial processes for the production of specialty chemicals, supporting the development of high-value products in the chemical industry.

Brand	TCI
CAS number	893440-50-1
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or powder, depending on the specific product formulation
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize inhalation risks. Avoid contact with incompatible materials such as strong oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this reagent. Proper storage and handling ensure the compound remains effective and safe for use in laboratory applications.

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