9-(2-Bromophenyl)-9H-carbazole TCI B4109

Chemical Identity

CAS No.: 902518-11-0
PubChem: CID 59465012·SID 354334664
Formula: C18H12BrN
Molecular weight: 322.2 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 9-(2-bromophenyl)carbazole
SMILES: C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=CC=CC=C4Br
InChIKey: KEWDVYIULXXMPP-UHFFFAOYSA-N

Rp 875.700,00

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9-(2-Bromophenyl)-9H-carbazole is a chemical compound widely used in organic synthesis reactions within laboratory settings. This heterocyclic building block plays a crucial role in the development of complex molecules with specific biological activities. Its unique structure combines a carbazole core with a bromophenyl group, making it a versatile intermediate in various chemical processes. In research environments, it is often employed as a key component in substitution reactions, coupling reactions, and aromatic reactions that require controlled reactivity and structural stability.

The compound is valued for its chemical stability and reactivity under controlled conditions. It exhibits non-volatile properties, which enhance its usability in long-term storage and repeated experimental applications. Its ability to participate in reactions with specific reagents and catalysts makes it a preferred choice for organic chemists. Additionally, its resistance to degradation under normal laboratory conditions ensures consistent performance across multiple experiments.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, compound development, and biological activity studies. Its role in creating new molecular structures and testing their potential applications makes it an essential tool for researchers. The compound is frequently utilized in academic and industrial settings to advance chemical innovation and scientific discovery.

TCI brochures (PDF)

Carbazoles 2025-06-27 · p. 5
Building Blocks for Organic Semiconductor 2026-03-24 · p. 18

Related TCI products

Organic synthesis reactions benefit from this compound's structural versatility and reactivity, enabling the creation of complex molecules with desired biological properties.
Coupling reactions often utilize this compound due to its ability to form stable intermediates under controlled conditions, enhancing reaction efficiency and yield.
Aromatic substitution reactions rely on this compound's stability and reactivity, allowing for precise control over reaction pathways and product formation.
Compound development projects use this material as a key building block to design new molecules with specific functional groups and biological activities.
Research into biological activity frequently incorporates this compound to test its potential in drug discovery and molecular interaction studies.

Brand	TCI
CAS number	902518-11-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its integrity. As a non-volatile compound, it does not require refrigeration but should be kept in a secure location to avoid contamination. In laboratory settings, it is essential to handle this material with care, using appropriate personal protective equipment to ensure safety. Due to its reactivity under specific conditions, it should be stored separately from incompatible substances to prevent unintended chemical interactions. Proper labeling and storage practices are crucial for maintaining the compound's effectiveness and safety in research applications.

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