5-Bromoindole-3-carboxaldehyde TCI B4840

Chemical Identity

CAS No.: 877-03-2
PubChem: CID 70137·SID 354333729
Formula: C9H6BrNO
Molecular weight: 224.05 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 5-bromo-1H-indole-3-carbaldehyde
SMILES: C1=CC2=C(C=C1Br)C(=CN2)C=O
InChIKey: PEENKJZANBYXNB-UHFFFAOYSA-N

Rp 769.650,00

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5-Bromoindole-3-carboxaldehyde is a chemical compound classified under the category of heterocyclic building blocks. It plays a crucial role in organic chemistry laboratories, serving as a foundational material for the synthesis of complex molecules with indole-based structures. This compound is widely used in various chemical reactions to construct molecules with specific functional properties, such as biological activity or optical characteristics. Its versatility makes it an essential reagent for researchers aiming to develop new compounds with tailored chemical properties.

The unique chemical structure of 5-Bromoindole-3-carboxaldehyde, featuring both a bromo group and a carbonyl group, contributes to its reactivity and functional versatility. These properties make it a preferred choice in substitution reactions, coupling reactions, and condensation reactions. The presence of the bromo group enhances its ability to participate in electrophilic substitution processes, while the aldehyde group allows for further functionalization. As a result, it is highly valued in the synthesis of heterocyclic compounds.

In Indonesian laboratories, 5-Bromoindole-3-carboxaldehyde is commonly used in organic chemistry research, including the development of new compounds with potential pharmaceutical or material applications. Its application extends to academic and industrial research settings, where it supports the creation of complex molecular structures. Researchers rely on this compound for its reliability and effectiveness in chemical synthesis processes.

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive bromo and aldehyde functional groups
Development of pharmaceuticals and materials through targeted molecular construction
Facilitation of coupling and condensation reactions in complex molecule formation
Support for research in biological activity and optical properties of synthesized compounds
Use in academic and industrial settings for advanced chemical experimentation

Brand	TCI
CAS number	877-03-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid, depending on the specific product variant
Storage	Store in a cool, dry place away from light and moisture

5-Bromoindole-3-carboxaldehyde should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. As a reactive chemical, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation is also essential when working with this compound to minimize inhalation risks. Storage conditions should be maintained to preserve its chemical integrity and ensure safe handling in laboratory settings.

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