Methyl 2-bromo-3-nitrobenzoate is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with both a bromine atom and a nitro group, as well as a methoxycarbonyl group (the ester functional group). Its molecular formula is C9H8BrN2O3, indicating the presence of carbon, hydrogen, bromine, nitrogen, and oxygen atoms. This compound typically appears as a yellow to brown solid and is soluble in organic solvents such as ethanol and acetone, but less soluble in water due to its hydrophobic aromatic structure. Methyl 2-bromo-3-nitrobenzoate is often utilized in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, owing to its reactivity and ability to undergo nucleophilic substitution reactions. Additionally, the presence of both the bromine and nitro groups makes it a valuable intermediate for further chemical transformations. As with many halogenated compounds, it is important to handle this substance with care, considering potential toxicity and environmental impact.

methyl 2-bromo-3-nitrobenzoate

5337-09-7: 2-bromo-3-nitroBenzoic acid methyl ester, Benzoic Acid, 2-Bromo-3-Nitro-, Methyl Ester, NSC 10344, NSC 409

Methyl 2-bromo-3-nitrobenzoate

Methyl 2-bromo-3-nitrobenzoate is a reactive monoxide compound that can be reduced with carbon monoxide to the corresponding nitrobenzene. The conversion is catalyzed by palladium ions in the presence of benzimidazoles. This reaction has been shown to be useful for the synthesis of benzimidazole derivatives.

CAS 5337-09-7: methyl 2-bromo-3-nitrobenzoate

Methyl 2-bromo-3-nitrobenzoate

Ref: IN-DA0039VH

Methyl 2-bromo-3-nitrobenzoate

Ref: 54-OR400515

Methyl 2-bromo-3-nitrobenzoate

Ref: 10-F212287

Methyl 2-bromo-3-nitrobenzoate

Ref: 3D-FM51031