5-bromo-3-fluoro-2-methoxyaniline
$325.00
CAS No.: 239122-51-1
Catalog No.: 194085
Purity: 95%
MF: C7H7BrFNO
MW: 220.041
Storage: 2-8 degree Celsius
SMILES: BrC=1C=C(C(=C(N)C1)OC)F
Catalog No.: 194085
Purity: 95%
MF: C7H7BrFNO
MW: 220.041
Storage: 2-8 degree Celsius
SMILES: BrC=1C=C(C(=C(N)C1)OC)F
5-bromo-3-fluoro-2-methoxyaniline; CAS No.: 239122-51-1; 5-bromo-3-fluoro-2-methoxyaniline. PROPERTIES: 5-bromo-3-fluoro-2-methoxyaniline is a crystalline solid. Its molecular formula is C7H7BrFNO, and the molecular weight is approximately 228.05 g/mol. The compound has a melting point of approximately 70-72 C. It is slightly soluble in water but dissolves well in organic solvents such as DMSO and DMF. For proper storage, it should be kept in a sealed container at 2-8 C, protected from light and moisture. As an aromatic amine compound containing bromine and fluorine atoms, it may have certain reactivity and toxicity. When handling it, protective gloves, eye protection, and a lab coat should be worn. In case of skin contact, washing with soap and water is necessary, and in case of eye contact, thorough rinsing with water is required. APPLICATIONS: In organic synthesis, 5-bromo-3-fluoro-2-methoxyaniline serves as an important intermediate. The amino group can undergo reactions such as acylation, sulfonation, and diazotization. The bromine and fluorine atoms provide sites for further substitution or coupling reactions, while the methoxy group can influence the electronic properties of the aromatic ring. In the pharmaceutical industry, derivatives of 5-bromo-3-fluoro-2-methoxyaniline can be explored as potential drug candidates. For instance, in the development of certain antiviral drugs, the unique substituents of this compound can be utilized to design drugs with enhanced antiviral activity and selectivity (as reported in medicinal chemistry journals). Furthermore, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in materials science and catalysis (as noted in organic chemistry research papers).
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