methyl 3-fluoro-4-hydroxymethylbenzoate
$200.00
CAS No.: 937636-18-5
Catalog No.: 194138
Purity: 95%
MF: C9H9FO3
MW: 184.166
Storage: 2-8 degree Celsius
SMILES: FC=1C=C(C(=O)OC)C=CC1CO
Catalog No.: 194138
Purity: 95%
MF: C9H9FO3
MW: 184.166
Storage: 2-8 degree Celsius
SMILES: FC=1C=C(C(=O)OC)C=CC1CO
methyl 3-fluoro-4-hydroxymethylbenzoate; CAS No.: 937636-18-5; methyl 3-fluoro-4-hydroxymethylbenzoate. PROPERTIES: methyl 3-fluoro-4-hydroxymethylbenzoate is a crystalline solid. Its molecular formula is C10H10FO3, and the molecular weight is approximately 194.19 g/mol. The compound has a melting point of approximately 60-62 C. It is moderately soluble in common organic solvents such as methanol and dimethylformamide, 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 compound containing a fluorine atom, a hydroxymethyl group, and 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 ingestion, medical attention should be sought immediately. APPLICATIONS: In organic synthesis, methyl 3-fluoro-4-hydroxymethylbenzoate serves as a valuable intermediate. The fluorine atom influences the electronic properties of the aromatic ring, the hydroxymethyl group can be converted to other functional groups such as ether or ester, 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 instance, in the development of certain antimicrobial agents, the structure of methyl 3-fluoro-4-hydroxymethylbenzoate 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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