methyl 2-bromo-2-(4-fluorophenyl)acetate

methyl 2-bromo-2-(4-fluorophenyl)acetate

methyl 2-bromo-4-chloro-5-fluorobenzoate

methyl 2-bromo-4-chloro-5-fluorobenzoate

methyl 2-bromo-3,4-difluorobenzoate

$340.00
CAS No.: 1805523-36-7
Catalog No.: 194118
Purity: 95%
MF: C8H5BrF2O2
MW: 251.026
Storage: 2-8 degree Celsius
SMILES: BrC1=C(C(=O)OC)C=CC(=C1F)F
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194118
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methyl 2-bromo-3,4-difluorobenzoate; CAS No.: 1805523-36-7; methyl 2-bromo-3,4-difluorobenzoate. PROPERTIES: methyl 2-bromo-3,4-difluorobenzoate is a crystalline solid. Its molecular formula is C9H6BrF2O2, and the molecular weight is approximately 252.05 g/mol. The compound has a melting point of approximately 45-47 C. It is moderately soluble in common organic solvents such as dichloromethane and ethyl acetate, but is poorly soluble in water. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a brominated and fluorinated aromatic compound containing an ester group, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, methyl 2-bromo-3,4-difluorobenzoate serves as a versatile intermediate. The bromine atom provides a site for substitution or coupling reactions, the two fluorine atoms influence the electronic properties of the aromatic ring, and the ester group can be hydrolyzed to a carboxylic acid. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain antimicrobial agents, the structure of methyl 2-bromo-3,4-difluorobenzoate can be modified to enhance the drug's antimicrobial activity and selectivity (as reported in medicinal chemistry journals). Additionally, 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 catalysis and sensing (as noted in organic chemistry research papers).

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