2-(3-Bromophenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborine TCI B3654

Chemical Identity

CAS No.: 927384-43-8
PubChem: CID 53384412·SID 125307607
Formula: C16H12BBrN2
Molecular weight: 323.0 g/mol
Purity: >98.0%(GC)(N)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-(3-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=C4)Br
InChIKey: RDGOAMRKYXEHHS-UHFFFAOYSA-N

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2-(3-Bromophenyl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborine is a specialized chemical compound used in various organometallic reactions, particularly in the synthesis of heterocyclic compounds and boron-based complexes. This compound plays a crucial role in laboratory settings where the manipulation of boron and nitrogen atoms is essential. Its unique molecular structure allows for versatile chemical interactions, making it a valuable tool in synthetic chemistry. The compound is often employed in research that requires precise control over reaction mechanisms and molecular reactivity.

The compound’s chemical properties, including its stability under controlled conditions and its sensitivity to moisture and air, make it a preferred choice for advanced chemical synthesis. Its ability to form complexes with transition metals and its reactivity in substitution reactions contribute to its popularity among researchers. The presence of aromatic groups and the boron-nitrogen framework enhances its utility in creating complex molecular structures. These characteristics enable it to be a key reagent in modern chemical research, particularly in the development of new pharmaceutical compounds.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and pharmaceutical applications. Its use is prevalent in academic and industrial research settings where the synthesis of complex molecules is required. Due to its unique reactivity and molecular structure, it is a favored reagent in studies related to drug development and advanced chemical synthesis. The compound’s role in these contexts highlights its importance in the field of chemical innovation.

TCI brochures (PDF)

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

Related TCI products

Used in the synthesis of heterocyclic compounds due to its ability to form stable boron-nitrogen complexes.
Applied in pharmaceutical research for the development of new drug molecules with complex structures.
Employed in organometallic chemistry to facilitate substitution reactions involving aromatic groups.
Utilized in transition metal complex formation due to its reactivity with metal ions.
Integrated into organic synthesis protocols requiring precise control over molecular reactivity and stability.

Brand	TCI
CAS number	927384-43-8
Molecular formula	—
Purity	—
Category	Chemistry > Organometallic Reagents > Organoboron [Organometallic Reagents]
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid, typically in crystalline or powder form
Storage	Requires storage in a dry, cool, and dark environment to prevent degradation

This compound should be stored in a dry, cool, and dark environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which can lead to degradation. The material is sensitive to humidity, so maintaining a controlled environment is essential. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment. It is advisable to store it away from incompatible substances to ensure safety. Proper labeling and storage conditions are crucial to preserving its effectiveness and ensuring safe handling in the laboratory.

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