3-Bromo-p-anisaldehyde TCI B1790

Chemical Identity

CAS No.: 34841-06-0
PubChem: CID 98662·SID 87564683
Formula: C8H7BrO2
Molecular weight: 215.04 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromo-4-methoxybenzaldehyde
SMILES: COC1=C(C=C(C=C1)C=O)Br
InChIKey: QMPNFQLVIGPNEI-UHFFFAOYSA-N

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3-Bromo-p-anisaldehyde is a chemical compound widely used in organic reactions for the synthesis of complex molecules. It serves as a fundamental building block in chemical laboratories, offering high reactivity and versatility in various synthetic pathways. This compound is commonly employed in research settings where the creation of aromatic and heterocyclic compounds is required. Its ability to participate in multiple reaction types makes it an essential reagent for chemists working on advanced synthetic projects.

The unique chemical properties of 3-Bromo-p-anisaldehyde make it a preferred choice for synthetic chemists. The presence of both a bromo group and an aldehyde functional group contributes to its reactivity. These groups enable the compound to engage in nucleophilic substitution, electrophilic addition, and condensation reactions. Its stable molecular structure ensures it remains effective under a range of reaction conditions, while its reactivity allows it to be a key player in the development of new chemical compounds.

In Indonesian laboratories, 3-Bromo-p-anisaldehyde is frequently used by researchers and students in higher education institutions and research organizations. It plays a vital role in the development of new compounds, catalyst testing, and organic chemistry research. Its availability supports the advancement of chemical studies and facilitates the execution of complex synthetic processes in both academic and industrial research environments.

Related TCI products

Organic synthesis for the creation of aromatic and heterocyclic compounds due to its reactive functional groups.
Nucleophilic substitution reactions as a versatile electrophilic substrate for synthetic transformations.
Catalyst testing in chemical processes where reactivity and structural modification are required.
Condensation reactions to form complex molecules through functional group interactions.
Research in chemical development for the synthesis of new compounds in academic and industrial settings.

Brand	TCI
CAS number	34841-06-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Solid or liquid depending on the specific formulation
Storage	Store in a cool, dry place away from light and incompatible substances

3-Bromo-p-anisaldehyde should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be kept away from strong bases, reducing agents, and other incompatible substances. Proper ventilation is essential when handling this compound to minimize exposure. Always wear appropriate personal protective equipment, including gloves, goggles, and a lab coat, to ensure safe handling in laboratory environments.

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