CAS 16791-41-6

2-BROMO-4,5-DIMETHOXYANILINE

Description:

2-Bromo-4,5-dimethoxyaniline is an organic compound characterized by the presence of a bromine atom and two methoxy groups attached to an aniline structure. Its molecular formula typically includes carbon, hydrogen, nitrogen, and bromine, reflecting its aromatic nature. The methoxy groups contribute to its solubility in organic solvents and influence its reactivity, particularly in electrophilic substitution reactions. The bromine substituent can also participate in further chemical transformations, making this compound useful in synthetic organic chemistry. It is often employed as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. The presence of the amino group (-NH2) allows for hydrogen bonding, which can affect its physical properties, such as melting and boiling points. Additionally, the compound may exhibit specific biological activities, which can be of interest in medicinal chemistry. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, 2-bromo-4,5-dimethoxyaniline is a versatile compound with significant applications in various chemical fields.

Formula: C₈H₁₀BrNO₂

Synonyms:

• 2-BROMO-4,5-DIMETHOXYANILINE
• Benzenamine, 2-bromo-4,5-dimethoxy-

Benzenamine, 2-bromo-4,5-dimethoxy-

CAS: 16791-41-6

Formula: C₈H₁₀BrNO₂

Purity: 97%

Molecular weight: 232.0745

Ref: IN-DA001XP7

2-Bromo-4,5-dimethoxyaniline

CAS: 16791-41-6

Formula: C₈H₁₀BrNO₂

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 232.077

Ref: 10-F465300

2-bromo-4,5-dimethoxyaniline

CAS: 16791-41-6

2-Bromo-4,5-dimethoxyaniline is a chemical compound that is used to optimize the synthesis of antimalarial agents. It has been shown that 2-bromo-4,5-dimethoxyaniline can be used as an efficient and selective synthetic intermediate for the preparation of benzene derivatives with biological properties. This chemical compound has been shown to be a mediation agent in biological systems and is also responsible for cross-coupling reactions between carbazoles and acridinium. The method for preparing this chemical compound involves a two step process involving alkylation and hydrolysis. The first step involves the preparation of dimethylformamide by reacting methyl iodide with formaldehyde in methanol. In the second step, acetyl chloride reacts with 2-bromoethanol in DMF to produce 2-bromo-4,5-dimethoxyaniline.

Formula: C₈H₁₀BrNO₂

Purity: Min. 95%

Molecular weight: 232.1 g/mol

Ref: 3D-RAA79141