(4,5-Dimethyl-3-thienyl)methanol is an organic compound characterized by its thienyl group, which is a five-membered aromatic ring containing sulfur. The presence of two methyl groups at the 4 and 5 positions of the thienyl ring contributes to its hydrophobic characteristics and can influence its reactivity and solubility in various solvents. The methanol functional group (-CH2OH) introduces a polar hydroxyl group, enhancing its potential for hydrogen bonding and increasing its solubility in polar solvents. This compound may exhibit interesting chemical properties, including potential reactivity in nucleophilic substitution reactions due to the presence of the hydroxyl group. Additionally, the structural features suggest that it could participate in various biological activities, making it of interest in medicinal chemistry. Its specific applications and behavior would depend on the context of its use, including its interactions with other chemical species and its stability under different conditions. Overall, (4,5-dimethyl-3-thienyl)methanol presents a unique combination of hydrophobic and hydrophilic characteristics, making it a versatile compound in organic synthesis and potential pharmaceutical applications.

(4,5-dimethyl-3-thienyl)methanol

119072-18-3: (4,5-Dimethyl-3-thienyl)methanol is an organic compound characterized by its thienyl group, which is a five-membered aromatic ring containing sulfur. The presence of two methyl groups at the 4 and 5 positions of the thienyl ring contributes to its hydrophobic characteristics and can influence its reactivity and solubility in various solvents. The methanol functional group (-CH2OH) introduces a polar hydroxyl group, enhancing its potential for hydrogen bonding and increasing its solubility in polar solvents. This compound may exhibit interesting chemical properties, including potential reactivity in nucleophilic substitution reactions due to the presence of the hydroxyl group. Additionally, the structural features suggest that it could participate in various biological activities, making it of interest in medicinal chemistry. Its specific applications and behavior would depend on the context of its use, including its interactions with other chemical species and its stability under different conditions. Overall, (4,5-dimethyl-3-thienyl)methanol presents a unique combination of hydrophobic and hydrophilic characteristics, making it a versatile compound in organic synthesis and potential pharmaceutical applications.

CAS 119072-18-3

(4,5-dimethyl-3-thienyl)methanol

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Ref: IN-DA000I5J

(4,5-Dimethylthiophen-3-yl)methanol

Ref: 3D-UEA07218