3-Bromo-5-nitrobenzaldehyde TCI B4982

Chemical Identity

CAS No.: 355134-13-3
PubChem: CID 16743966·SID 468590535
Formula: C7H4BrNO3
Molecular weight: 230.02 g/mol
Purity: >96.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromo-5-nitrobenzaldehyde
SMILES: C1=C(C=C(C=C1[N+](=O)[O-])Br)C=O
InChIKey: OUDCOMBHRXKPIJ-UHFFFAOYSA-N

Rp 637.350,00

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3-Bromo-5-nitrobenzaldehyde is a chemical compound widely used as a building block in the synthesis of complex molecules. It is a versatile reagent in organic chemistry, particularly in laboratory settings where the development of new compounds is essential. This compound is commonly employed in various synthetic pathways due to its functional group diversity, which includes a bromo and nitro substituent on a benzaldehyde core. Its presence in chemical libraries makes it a valuable resource for researchers aiming to explore new chemical structures and biological activities.

The compound's high reactivity and functional group versatility make it a preferred choice in laboratory applications. Its aromatic structure, combined with the electron-withdrawing nitro group and the electrophilic bromo substituent, allows it to participate in a wide range of chemical reactions, such as electrophilic substitution and nitration. Additionally, its solubility in common organic solvents like ethyl acetate and acetone enhances its usability in synthetic processes. These properties make it an essential reagent for organic synthesis and drug development.

In Indonesian laboratories, 3-Bromo-5-nitrobenzaldehyde is a key component in research focused on pharmaceutical and organic chemistry. Its availability and chemical reactivity make it a popular choice for scientists working on the synthesis of bioactive compounds. It is frequently used in academic and industrial research settings, contributing to the development of new therapeutic agents and chemical materials. Its role in synthetic chemistry ensures its continued use in both educational and applied research contexts.

Related TCI products

Organic Synthesis: This compound is ideal for creating complex molecules due to its reactive functional groups, making it a key reagent in synthetic pathways.
Pharmaceutical Research: Its ability to participate in various reactions makes it suitable for the development of new drug compounds with biological activity.
Nitration Reactions: The nitro group enhances its utility in nitration processes, allowing for the synthesis of nitro derivatives with specific properties.
Electrophilic Substitution: The bromo substituent enables it to act as an electrophilic reagent in substitution reactions, expanding its synthetic applications.
Compound Library Development: Its structural complexity and reactivity make it a valuable component in chemical libraries for drug discovery and research.

Brand	TCI
CAS number	355134-13-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-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 incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to store it separately from strong bases and reducing agents to avoid potential chemical reactions. In laboratory settings, it should be kept in a well-ventilated area to minimize inhalation risks. Always follow standard laboratory safety protocols when working with this compound to ensure safe handling and storage.

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