2-(2-Bromophenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborine TCI B3653

Chemical Identity

CAS No.: 927384-42-7
PubChem: CID 53384411·SID 125307606
Formula: C16H12BBrN2
Molecular weight: 323.0 g/mol
Purity: >98.0%(GC)(N)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-(2-bromophenyl)-2,4-diaza-3-boratricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene
SMILES: B1(NC2=CC=CC3=C2C(=CC=C3)N1)C4=CC=CC=C4Br
InChIKey: VHWWJBPYVUEFBM-UHFFFAOYSA-N

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2-(2-Bromophenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborine is a complex organic compound widely used in laboratory settings for its unique chemical properties. It belongs to the class of organoboron compounds and is commonly employed in synthetic chemistry for the preparation of heterocyclic and boron-containing molecules. This reagent plays a vital role in substitution reactions and catalytic processes, where the presence of boron atoms is essential for reaction mechanisms. Its versatility makes it a valuable tool in both academic and industrial research environments.

The compound is favored for its ability to participate in both electrophilic and nucleophilic reactions, offering researchers control over reaction outcomes. Its chemical structure allows it to interact with various functional groups, making it suitable for a wide range of synthetic applications. The stability and reactivity of this compound are carefully balanced, enabling precise control in complex reaction systems. These characteristics make it an essential component in the synthesis of advanced organic molecules.

In Indonesian laboratories, this compound is frequently used in organic chemistry research, particularly in the development of new materials and complex molecular structures. It is a key reagent in the synthesis of heterocyclic compounds and boron-based derivatives. Researchers in educational and industrial settings rely on its predictable behavior and chemical versatility to achieve desired outcomes in their experiments. Its applications span across various fields, including pharmaceutical and materials science research.

TCI brochures (PDF)

Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 20
Boron Compounds 2025-10-07 · p. 21

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactivity and ability to form stable intermediates.
Catalytic reactions requiring boron-based reagents for enhanced reaction efficiency and selectivity.
Development of new materials through controlled chemical modifications and functional group interactions.
Research in pharmaceutical chemistry for the synthesis of boron-containing drug candidates.
Investigation of electrophilic and nucleophilic reaction mechanisms in advanced organic chemistry studies.

Brand	TCI
CAS number	927384-42-7
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various quantities as per standard laboratory supply formats.
Physical form	Solid or liquid, depending on the specific product formulation.
Storage	—

This compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers made of materials compatible with its chemical nature to prevent contamination and degradation. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation and to avoid exposure to incompatible substances. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the compound.

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