4-Bromo-1H-imidazole TCI B3280

Chemical Identity

CAS No.: 2302-25-2
PubChem: CID 96125·SID 87560690
Formula: C3H3BrN2
Molecular weight: 146.97 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 5-bromo-1H-imidazole
SMILES: C1=C(NC=N1)Br
InChIKey: FHZALEJIENDROK-UHFFFAOYSA-N

Rp 505.050,00

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4-Bromo-1H-imidazole is a chemical compound classified under the heterocyclic category, featuring an imidazole core with a bromine substituent at the fourth position. This compound plays a crucial role in laboratory settings as a building block for the synthesis of complex molecules, particularly in organic chemistry and pharmacology. Its versatility allows it to be modified through various chemical reactions to produce biologically active compounds, making it a valuable resource for researchers.

The compound is known for its reactivity, especially at the brominated site, which makes it ideal for nucleophilic substitution, coupling reactions, and halogenation processes. Its polar nature enables solubility in organic solvents such as ethyl acetate and acetone, enhancing its utility in diverse synthetic pathways. These properties contribute to its widespread use in both academic and industrial research environments.

In Indonesian laboratories, 4-Bromo-1H-imidazole is commonly used in the development of pharmaceutical compounds and organic synthesis projects. Its stability and reactivity make it a preferred choice for chemists and pharmacologists seeking to explore new molecular structures and drug candidates. Its presence in research labs supports the advancement of chemical and medicinal science in the region.

Related TCI products

Organic synthesis projects benefit from 4-Bromo-1H-imidazole due to its reactivity and ability to participate in nucleophilic substitution reactions, enabling the creation of complex molecular structures.
Pharmaceutical research utilizes this compound as a starting material for the synthesis of bioactive molecules, supporting the development of new drug candidates.
Heterocyclic compound studies rely on 4-Bromo-1H-imidazole as a model compound for understanding the behavior of imidazole derivatives in various chemical environments.
Halogenation reactions are enhanced by the bromine substituent, making this compound a key reagent in the synthesis of halogenated heterocyclic compounds.
Coupling reactions in synthetic chemistry are facilitated by the compound’s structural versatility, allowing for the formation of diverse molecular architectures.

Brand	TCI
CAS number	2302-25-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

4-Bromo-1H-imidazole should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and degradation. Due to its polar nature, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is not classified as hazardous under standard conditions, but its reactivity necessitates careful handling during chemical reactions. Proper storage and handling protocols help preserve the compound’s integrity and ensure safe usage in laboratory settings.

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