6-Bromoindole-2-carboxylic Acid TCI B4334

Chemical Identity

CAS No.: 16732-65-3
PubChem: CID 4011696·SID 253661991
Formula: C9H6BrNO2
Molecular weight: 240.05 g/mol
Purity: >97.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 6-bromo-1H-indole-2-carboxylic acid
SMILES: C1=CC2=C(C=C1Br)NC(=C2)C(=O)O
InChIKey: SVBVYRYROZWKNJ-UHFFFAOYSA-N

Rp 2.491.650,00

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6-Bromoindole-2-carboxylic Acid is a chemical compound widely used in organic synthesis reactions, particularly in the development of complex heterocyclic compounds. This versatile building block is commonly found in chemical laboratories as a foundational material for creating indole-based structures with diverse applications in pharmacology and industry. Its role as a substrate or reactant enables participation in substitution, reduction, and catalytic reactions, making it an essential component in synthetic pathways.

The unique molecular structure of 6-Bromoindole-2-carboxylic Acid, featuring a bromo group at position 6 and a carboxylic acid group at position 2, contributes to its reactivity and functional versatility. The presence of the bromo group enhances its ability to undergo nucleophilic substitution reactions, making it a preferred choice for chemists seeking to modify indole frameworks. This chemical’s reactivity and structural specificity make it a valuable tool in both academic and industrial research settings.

In Indonesian laboratories, 6-Bromoindole-2-carboxylic Acid is frequently utilized in chemical, pharmaceutical, and biochemical research. It is a key reagent in the development of new compounds with potential applications in drug discovery and material science. Its availability and chemical properties make it a standard component in the inventory of research institutions and academic laboratories across Indonesia.

Related TCI products

Organic synthesis of heterocyclic compounds due to its indole core and reactive bromo group.
Development of pharmaceuticals and bioactive molecules through functional group modification.
Catalytic reactions where bromoindole derivatives act as intermediates or substrates.
Structural studies of indole-based compounds for medicinal chemistry applications.
Research in biochemical pathways involving indole derivatives and their biological activity.

Brand	TCI
CAS number	16732-65-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

6-Bromoindole-2-carboxylic Acid should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and potential degradation. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn. Avoid contact with incompatible substances, and ensure proper disposal according to local regulations. Proper storage and handling practices help preserve the compound’s effectiveness and safety in laboratory settings.

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