4-Bromo-3-nitrobenzaldehyde TCI B5101

Chemical Identity

CAS No.: 163596-75-6
PubChem: CID 808792·SID 354333570
Formula: C7H4BrNO3
Molecular weight: 230.02 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-bromo-3-nitrobenzaldehyde
SMILES: C1=CC(=C(C=C1C=O)[N+](=O)[O-])Br
InChIKey: SAFSVELFSYQXOV-UHFFFAOYSA-N

Rp 717.150,00

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4-Bromo-3-nitrobenzaldehyde is a versatile organic compound widely used in laboratory settings for its reactivity and structural versatility. As a key building block in synthetic chemistry, it serves as a foundational material for the creation of more complex molecules. This compound is particularly valuable in organic synthesis due to its aromatic structure, which provides a stable yet reactive platform for further chemical modifications. Its presence in Indonesian laboratories underscores its importance in advancing chemical research and development.

The compound’s unique properties make it a preferred choice for chemists. The combination of a bromo group and a nitro group imparts specific electronic characteristics that influence its reactivity. The nitro group acts as an electron-withdrawing group, enhancing the electrophilicity of the molecule, while the bromo group contributes to the stability of the structure. These characteristics make it highly suitable for substitution reactions and reduction processes, allowing for precise control over the synthesis of target compounds.

In Indonesian laboratories, 4-Bromo-3-nitrobenzaldehyde is commonly used in organic chemistry research. It is frequently employed in the development of new compounds and the modification of molecular structures. Its reactivity and functional groups make it an essential tool for chemists working on complex synthetic pathways. This compound is integral to the work of researchers focused on creating novel chemical entities with specific properties.

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Organic synthesis applications benefit from its aromatic structure and reactive functional groups, enabling the creation of complex molecules.
It is ideal for substitution reactions due to the presence of bromo and nitro groups, which influence reactivity and selectivity.
Reduction reactions often utilize this compound as a starting material, allowing for the formation of more complex molecular frameworks.
It supports the development of new chemical compounds in research settings, offering a reliable building block for synthetic pathways.
Its use in molecular modification projects allows for the tailored design of compounds with specific functional properties.

Brand	TCI
CAS number	163596-75-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can lead to degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Storage away from incompatible substances is essential to avoid any potential chemical interactions. In laboratory settings, it should be kept in a designated chemical storage area that complies with safety regulations. Proper labeling of containers is also crucial for safe handling and easy identification.

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