5-Bromo-2-nitrobenzaldehyde TCI B4192

Chemical Identity

CAS No.: 20357-20-4
PubChem: CID 97233·SID 253660039
Formula: C7H4BrNO3
Molecular weight: 230.02 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 5-bromo-2-nitrobenzaldehyde
SMILES: C1=CC(=C(C=C1Br)C=O)[N+](=O)[O-]
InChIKey: UFRVBZVJVRHSNR-UHFFFAOYSA-N

Rp 1.035.300,00

~~Rp 723.450,00~~ Rp 1.035.300,00

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5-Bromo-2-nitrobenzaldehyde is a chemical compound widely used as a foundational building block in organic synthesis. Its aromatic structure, combined with bromo and nitro functional groups, makes it a versatile reagent in laboratory settings. This compound plays a crucial role in the development of complex molecules, particularly in research and development environments where precise chemical transformations are required. Its presence in various synthetic pathways highlights its importance in modern chemical research.

The compound's unique chemical properties, including its high reactivity and stability, make it a preferred choice for chemists. The presence of both electron-withdrawing and electron-donating groups enhances its ability to participate in a wide range of reactions, such as electrophilic and nucleophilic substitutions. These characteristics allow it to be used in multiple synthetic strategies, making it a valuable tool for researchers aiming to create new compounds with specific functional groups.

In Indonesian laboratories, 5-Bromo-2-nitrobenzaldehyde is commonly used in organic chemistry research, particularly in academic and research institutions. Its role in the synthesis of heterocyclic compounds and functionalized molecules is well established. It is frequently employed in projects that require the construction of complex molecular frameworks, supporting both educational and applied research initiatives.

Related TCI products

Organic synthesis projects benefit from this compound due to its reactivity and versatility in forming complex molecular structures.
It is ideal for electrophilic substitution reactions because of its electron-withdrawing nitro group and electron-donating bromo group.
Researchers use it in the development of heterocyclic compounds due to its ability to participate in nucleophilic reactions.
It supports the creation of functionalized molecules in academic and industrial research settings.
Its stability and reactivity make it suitable for oxidation and reduction reactions in synthetic pathways.

Brand	TCI
CAS number	20357-20-4
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 place, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity, it should be kept away from incompatible substances such as strong bases and reducing agents. Proper ventilation is essential when handling this material to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is advised to maintain the compound's integrity and safety.

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