3-Bromo-5-nitrobenzoic Acid TCI B3370

Chemical Identity

CAS No.: 6307-83-1
PubChem: CID 239336·SID 87560804
Formula: C7H4BrNO4
Molecular weight: 246.01 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

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

Rp 1.008.000,00

~~Rp 720.300,00~~ Rp 1.008.000,00

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3-Bromo-5-nitrobenzoic Acid is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a key building block in the development of complex chemical structures, enabling chemists to perform various substitution and functionalization reactions. This compound is commonly found in chemical laboratories, where it plays a vital role in the synthesis of a wide range of organic compounds. Its presence in research and development processes highlights its importance in both academic and industrial chemical applications.

The compound’s chemical properties, including its aromatic structure and the presence of bromo and nitro groups, make it a preferred choice for synthetic chemists. These functional groups contribute to its reactivity, allowing it to participate in electrophilic substitution and reduction reactions. Its stability under certain conditions further enhances its utility in laboratory environments. The combination of these properties makes it an essential reagent for those working on high-reactivity chemical syntheses.

In Indonesian laboratories, 3-Bromo-5-nitrobenzoic Acid is frequently used in organic chemistry research, particularly in the synthesis of synthetic compounds and the development of new chemical products. Its versatility and reactivity make it a valuable tool for scientists aiming to explore diverse chemical reactions and create novel molecular structures. Its application in both academic and industrial research underscores its significance in the chemical sciences.

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Organic synthesis applications benefit from its reactivity and functional group versatility, enabling the creation of complex molecular structures.
It is ideal for electrophilic substitution reactions due to its bromo and nitro substituents, which enhance reactivity in synthetic pathways.
In the development of pharmaceutical compounds, its ability to undergo reduction reactions makes it a valuable intermediate in drug synthesis.
It supports the preparation of functionalized aromatic compounds, which are essential in materials science and polymer chemistry.
Its use in academic research helps students and scientists explore fundamental chemical reactions and synthetic methodologies.

Brand	TCI
CAS number	6307-83-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent moisture absorption and contamination. Due to its bromo and nitro groups, it may react with certain substances, so it should be handled with care in a well-ventilated area. Avoid exposure to heat or direct sunlight to prevent degradation. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling to ensure laboratory safety. Regular monitoring of storage conditions is essential to maintain the integrity of the compound.

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