(5-Phenylfuran-2-yl)methanol is an organic compound characterized by its furan and phenyl functional groups. It features a furan ring, which is a five-membered aromatic heterocycle containing one oxygen atom, and a phenyl group, which is a benzene ring substituent. The presence of the hydroxymethyl (-CH2OH) group indicates that it is an alcohol, contributing to its potential reactivity and solubility in polar solvents. This compound may exhibit interesting chemical properties, such as the ability to participate in hydrogen bonding due to the hydroxyl group, which can influence its boiling point and solubility in various solvents. Additionally, the aromatic nature of the phenyl group can provide stability and influence the compound's electronic properties. (5-Phenylfuran-2-yl)methanol may have applications in organic synthesis, medicinal chemistry, or as a building block for more complex molecules, although specific applications would depend on further research into its biological activity and reactivity.

(5-phenylfuran-2-yl)methanol

22078-90-6: (5-Phenylfuran-2-yl)methanol is an organic compound characterized by its furan and phenyl functional groups. It features a furan ring, which is a five-membered aromatic heterocycle containing one oxygen atom, and a phenyl group, which is a benzene ring substituent. The presence of the hydroxymethyl (-CH2OH) group indicates that it is an alcohol, contributing to its potential reactivity and solubility in polar solvents. This compound may exhibit interesting chemical properties, such as the ability to participate in hydrogen bonding due to the hydroxyl group, which can influence its boiling point and solubility in various solvents. Additionally, the aromatic nature of the phenyl group can provide stability and influence the compound's electronic properties. (5-Phenylfuran-2-yl)methanol may have applications in organic synthesis, medicinal chemistry, or as a building block for more complex molecules, although specific applications would depend on further research into its biological activity and reactivity.

CAS 22078-90-6

(5-phenylfuran-2-yl)methanol

(5-Phenyl-furan-2-yl)-methanol

Ref: 10-F025229