2-Bromo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine TCI B5077

Chemical Identity

CAS No.: 651358-83-7
PubChem: CID 12177444·SID 354333453
Formula: C11H15BBrNO2
Molecular weight: 283.96 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
SMILES: B1(OC(C(O1)(C)C)(C)C)C2=NC(=CC=C2)Br
InChIKey: OAVRLCKBKDMGGW-UHFFFAOYSA-N

Rp 2.359.350,00

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2-Bromo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a specialized organic compound widely used in laboratory settings for its unique reactivity and structural versatility. It belongs to the organoboron reagent category, which plays a crucial role in various synthetic processes, particularly in cross-coupling reactions and S-N coupling. This compound is essential for the synthesis of complex heterocyclic compounds and halogenated derivatives, making it a valuable tool for chemists working on advanced organic synthesis. Its ability to participate in metal-mediated reactions enhances its utility in creating new molecular structures with high functional group diversity.

One of the key properties that make this compound a preferred choice is its stability under controlled conditions, combined with its reactivity towards specific chemical environments. It exhibits a high affinity for transition metals, which is critical in catalytic processes that require precise control over reaction pathways. Additionally, its molecular structure allows for efficient coupling reactions, which are fundamental in the development of pharmaceuticals and materials science. The compound’s compatibility with polar solvents and its ability to maintain chemical integrity during synthesis make it a reliable reagent for laboratory use.

In Indonesian laboratories, this compound is commonly used by researchers and scientists in the fields of pharmacology and material science. Its availability and adherence to international quality standards make it a preferred choice for those engaged in complex synthesis projects. The compound’s role in creating new compounds with potential applications in drug development and advanced materials underscores its importance in modern chemical research.

TCI brochures (PDF)

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

Related TCI products

S-N coupling reactions for the synthesis of complex heterocyclic compounds due to its reactivity and compatibility with transition metals.
Cross-coupling reactions in organic synthesis to form new carbon-carbon bonds with high efficiency and selectivity.
Development of halogenated derivatives for pharmaceutical applications requiring precise functional group manipulation.
Synthesis of advanced materials with specific structural properties through controlled chemical reactions.
Research in pharmacology for the creation of novel drug candidates with targeted molecular structures and functionalities.

Brand	TCI
CAS number	651358-83-7
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	As available
Physical form	Solid (may vary depending on supplier)
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, which may affect its reactivity. Due to its potential reactivity under certain conditions, it should be handled with appropriate laboratory safety measures, such as using gloves and a fume hood when necessary. The compound is best stored in airtight containers made of materials compatible with its chemical nature, such as glass or high-density polyethylene. Regular monitoring of storage conditions is advised to ensure optimal performance and safety in laboratory settings.

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