Phenol, 4-(3-thienylmethyl)-, also known by its CAS number 179018-41-8, is an organic compound characterized by the presence of a phenolic hydroxyl group (-OH) attached to a benzene ring, along with a thienylmethyl substituent. The thienyl group, derived from thiophene, introduces a five-membered aromatic ring containing sulfur, which contributes to the compound's unique chemical properties. This substance typically exhibits moderate solubility in organic solvents and may show limited solubility in water due to the hydrophobic nature of the thienyl group. Its structure suggests potential for various chemical reactivity, including electrophilic substitution and hydrogen bonding, which can influence its behavior in biological systems and synthetic applications. Additionally, compounds with similar structures are often studied for their potential pharmacological activities, including antimicrobial and anti-inflammatory properties. As with many phenolic compounds, it may also exhibit antioxidant activity, making it of interest in medicinal chemistry and materials science.

Phenol, 4-(3-thienylmethyl)-

179018-41-8: Phenol, 4-(3-thienylmethyl)-, also known by its CAS number 179018-41-8, is an organic compound characterized by the presence of a phenolic hydroxyl group (-OH) attached to a benzene ring, along with a thienylmethyl substituent. The thienyl group, derived from thiophene, introduces a five-membered aromatic ring containing sulfur, which contributes to the compound's unique chemical properties. This substance typically exhibits moderate solubility in organic solvents and may show limited solubility in water due to the hydrophobic nature of the thienyl group. Its structure suggests potential for various chemical reactivity, including electrophilic substitution and hydrogen bonding, which can influence its behavior in biological systems and synthetic applications. Additionally, compounds with similar structures are often studied for their potential pharmacological activities, including antimicrobial and anti-inflammatory properties. As with many phenolic compounds, it may also exhibit antioxidant activity, making it of interest in medicinal chemistry and materials science.

CAS 179018-41-8

Phenol, 4-(3-thienylmethyl)-

4-[(Thiophen-3-yl)methyl]phenol

Ref: 3D-EHA01841