methyl 2-chloro-5-fluoro-3-methylbenzoate
$300.00
CAS No.: 1805112-73-5
Catalog No.: 194123
Purity: 95%
MF: C9H8ClFO2
MW: 202.612
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C(=O)OC)C=C(C=C1C)F
Catalog No.: 194123
Purity: 95%
MF: C9H8ClFO2
MW: 202.612
Storage: 2-8 degree Celsius
SMILES: ClC1=C(C(=O)OC)C=C(C=C1C)F
methyl 2-chloro-5-fluoro-3-methylbenzoate; CAS No.: 1805112-73-5; methyl 2-chloro-5-fluoro-3-methylbenzoate. PROPERTIES: methyl 2-chloro-5-fluoro-3-methylbenzoate is a crystalline solid. Its molecular formula is C10H8ClFO2, and the molecular weight is approximately 211.62 g/mol. The compound has a melting point of approximately 40-42 C. It is moderately soluble in common organic solvents such as ethyl acetate and tetrahydrofuran, 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 chlorinated and fluorinated aromatic compound containing an ester group and a methyl 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-chloro-5-fluoro-3-methylbenzoate serves as a versatile intermediate. The chlorine and fluorine atoms provide sites for substitution reactions, the methyl group offers steric effects, 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 antiviral drugs, the structure of methyl 2-chloro-5-fluoro-3-methylbenzoate can be modified to enhance the drug's antiviral activity and pharmacokinetic properties (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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