1-(3-Bromofuran-2-yl)ethanol is an organic compound characterized by the presence of a furan ring substituted with a bromine atom and a hydroxyl group attached to an ethyl chain. The furan ring contributes to the compound's aromatic properties, while the bromine substitution enhances its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. The hydroxyl group (-OH) indicates that it is an alcohol, which can participate in hydrogen bonding, influencing its solubility in polar solvents. This compound may exhibit biological activity due to the presence of the furan moiety, which is often associated with various pharmacological properties. Its molecular structure allows for potential applications in medicinal chemistry, agrochemicals, and material science. Additionally, the presence of the bromine atom can facilitate further functionalization, making it a versatile intermediate in organic synthesis. Safety data should be consulted, as brominated compounds can pose health risks, and appropriate handling procedures should be followed.

1-(3-Bromofuran-2-yl)ethanol

67170-98-3: 1-(3-Bromofuran-2-yl)ethanol is an organic compound characterized by the presence of a furan ring substituted with a bromine atom and a hydroxyl group attached to an ethyl chain. The furan ring contributes to the compound's aromatic properties, while the bromine substitution enhances its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. The hydroxyl group (-OH) indicates that it is an alcohol, which can participate in hydrogen bonding, influencing its solubility in polar solvents. This compound may exhibit biological activity due to the presence of the furan moiety, which is often associated with various pharmacological properties. Its molecular structure allows for potential applications in medicinal chemistry, agrochemicals, and material science. Additionally, the presence of the bromine atom can facilitate further functionalization, making it a versatile intermediate in organic synthesis. Safety data should be consulted, as brominated compounds can pose health risks, and appropriate handling procedures should be followed.

CAS 67170-98-3

1-(3-Bromofuran-2-yl)ethanol

2-Furanmethanol, 3-bromo-a-methyl-

Ref: IN-DA01K53B

1-(3-Bromofuran-2-yl)ethanol

Ref: 54-OR71027

1-(3-Bromofuran-2-yl)ethanol

Ref: 10-F633449