4-Methyl-2-oxo-2H-chromen-7-yl chloroacetate is a chemical compound belonging to the class of coumarin derivatives. It features a coumarin backbone, characterized by a benzopyrone structure, which contributes to its aromatic properties and potential biological activity. The presence of a methyl group at the 4-position and a chloroacetate moiety enhances its reactivity and solubility in organic solvents. This compound is typically a yellow to light brown solid, exhibiting moderate stability under standard conditions. Its functional groups suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activities often associated with coumarin derivatives, such as anticoagulant, anti-inflammatory, and antimicrobial properties. Additionally, the chloroacetate group may facilitate further chemical modifications, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 4-methyl-2-oxo-2H-chromen-7-yl chloroacetate represents a significant compound for research and development in various chemical and pharmaceutical applications.

4-methyl-2-oxo-2H-chromen-7-yl chloroacetate

105738-24-7: 4-Methyl-2-oxo-2H-chromen-7-yl chloroacetate is a chemical compound belonging to the class of coumarin derivatives. It features a coumarin backbone, characterized by a benzopyrone structure, which contributes to its aromatic properties and potential biological activity. The presence of a methyl group at the 4-position and a chloroacetate moiety enhances its reactivity and solubility in organic solvents. This compound is typically a yellow to light brown solid, exhibiting moderate stability under standard conditions. Its functional groups suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological activities often associated with coumarin derivatives, such as anticoagulant, anti-inflammatory, and antimicrobial properties. Additionally, the chloroacetate group may facilitate further chemical modifications, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 4-methyl-2-oxo-2H-chromen-7-yl chloroacetate represents a significant compound for research and development in various chemical and pharmaceutical applications.

CAS 105738-24-7

4-methyl-2-oxo-2H-chromen-7-yl chloroacetate

4-Methyl-2-oxo-2H-chromen-7-yl chloroacetate

Ref: IN-DA007FH8

4-methyl-2-oxo-2H-chromen-7-yl chloroacetate

Ref: 10-F369196