Methyl 4-bromo-5-chloro-2-nitrobenzoate is an organic compound characterized by its aromatic structure, which includes a benzoate moiety substituted with various halogen and nitro groups. This compound features a methyl ester functional group, contributing to its solubility in organic solvents. The presence of bromine and chlorine atoms introduces significant electronegativity, influencing the compound's reactivity and polarity. The nitro group, known for its electron-withdrawing properties, further enhances the compound's potential for electrophilic substitution reactions. Methyl 4-bromo-5-chloro-2-nitrobenzoate is typically used in synthetic organic chemistry as an intermediate for the preparation of more complex molecules, including pharmaceuticals and agrochemicals. Its unique combination of substituents can also impart specific biological activities, making it of interest in medicinal chemistry. Safety considerations should be taken into account due to the presence of halogens and nitro groups, which may pose environmental and health risks. Overall, this compound exemplifies the intricate interplay of functional groups in determining the chemical behavior and applications of aromatic compounds.

methyl 4-bromo-5-chloro-2-nitrobenzoate

1416374-90-7: Methyl 4-bromo-5-chloro-2-nitrobenzoate is an organic compound characterized by its aromatic structure, which includes a benzoate moiety substituted with various halogen and nitro groups. This compound features a methyl ester functional group, contributing to its solubility in organic solvents. The presence of bromine and chlorine atoms introduces significant electronegativity, influencing the compound's reactivity and polarity. The nitro group, known for its electron-withdrawing properties, further enhances the compound's potential for electrophilic substitution reactions. Methyl 4-bromo-5-chloro-2-nitrobenzoate is typically used in synthetic organic chemistry as an intermediate for the preparation of more complex molecules, including pharmaceuticals and agrochemicals. Its unique combination of substituents can also impart specific biological activities, making it of interest in medicinal chemistry. Safety considerations should be taken into account due to the presence of halogens and nitro groups, which may pose environmental and health risks. Overall, this compound exemplifies the intricate interplay of functional groups in determining the chemical behavior and applications of aromatic compounds.

CAS 1416374-90-7

methyl 4-bromo-5-chloro-2-nitrobenzoate

Benzoic acid, 4-bromo-5-chloro-2-nitro-, methyl ester

Ref: IN-DA001GRP

Methyl 4-bromo-5-chloro-2-nitrobenzoate

Ref: 54-OR1040189

2-NITRO-4-BROMO-5-CHLOROBENZOIC ACID METHYL ESTER

Ref: 10-F859414