Methyl 4-Bromo-3-nitrobenzoate TCI M2596

Chemical Identity

CAS No.: 2363-16-8
PubChem: CID 2736829·SID 253660892
Formula: C8H6BrNO4
Molecular weight: 260.04 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 4-bromo-3-nitrobenzoate
SMILES: COC(=O)C1=CC(=C(C=C1)Br)[N+](=O)[O-]
InChIKey: BNNDHGPPQZVKMX-UHFFFAOYSA-N

Rp 743.400,00

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Methyl 4-Bromo-3-nitrobenzoate is a chemical compound widely used as a building block in organic synthesis. It serves as a versatile intermediate in the creation of complex organic molecules, particularly in laboratory settings where precise chemical reactions are required. This compound is commonly utilized in substitution, reduction, and electrophilic reactions, making it an essential tool for chemists working on functional group transformations. Its role in the laboratory is critical for the development of new compounds with specific structural and functional properties.

The compound's chemical stability and controlled reactivity make it a preferred choice for researchers. Its aromatic structure, combined with bromo and nitro substituents, provides unique electronic and reactive characteristics. These properties allow it to participate in a variety of chemical reactions, especially in the synthesis of heterocyclic compounds and functionalized molecules. The predictable behavior of Methyl 4-Bromo-3-nitrobenzoate ensures reliable results in experimental processes, contributing to its popularity in both academic and industrial research.

In Indonesian laboratories, this compound is frequently used in research conducted by universities, research institutions, and pharmaceutical industries. Its availability and reliability make it a go-to material for chemists aiming to produce high-quality chemical products. The compound's role in advancing chemical research in Indonesia underscores its importance in the scientific community.

Related TCI products

Organic synthesis of heterocyclic compounds due to its aromatic structure and reactive substituents.
Functional group modification in complex molecule development through substitution and reduction reactions.
Pharmaceutical research for the creation of drug precursors and intermediate compounds.
Analytical chemistry applications where precise chemical reactivity is required for compound identification.
Teaching and research in academic institutions for demonstrating chemical reaction mechanisms and synthesis techniques.

Brand	TCI
CAS number	2363-16-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid (exact form may vary depending on supplier)
Storage	Store in a cool, dry place away from light and incompatible substances

Methyl 4-Bromo-3-nitrobenzoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to heat, direct sunlight, and incompatible materials like strong acids or bases. Regular inspection of storage conditions ensures the compound remains in optimal condition for use in research applications.

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