2,4-Dimethylthiophene-3-ol is an organic compound characterized by its thiophene ring structure, which includes a sulfur atom within a five-membered aromatic ring. This compound features two methyl groups attached to the 2 and 4 positions of the thiophene ring and a hydroxyl (-OH) group at the 3 position, contributing to its classification as an alcohol. The presence of the hydroxyl group imparts polar characteristics, enhancing its solubility in polar solvents while maintaining some hydrophobic properties due to the thiophene structure. This compound is typically colorless to pale yellow and may have a distinctive odor, often associated with thiophene derivatives. It is used in various applications, including organic synthesis and as a potential intermediate in the production of pharmaceuticals and agrochemicals. The compound's reactivity is influenced by the electron-donating nature of the methyl groups and the electron-withdrawing nature of the hydroxyl group, making it a versatile building block in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

2,4-Dimethylthiophene-3-ol

121144-97-6: 2,4-Dimethylthiophene-3-ol is an organic compound characterized by its thiophene ring structure, which includes a sulfur atom within a five-membered aromatic ring. This compound features two methyl groups attached to the 2 and 4 positions of the thiophene ring and a hydroxyl (-OH) group at the 3 position, contributing to its classification as an alcohol. The presence of the hydroxyl group imparts polar characteristics, enhancing its solubility in polar solvents while maintaining some hydrophobic properties due to the thiophene structure. This compound is typically colorless to pale yellow and may have a distinctive odor, often associated with thiophene derivatives. It is used in various applications, including organic synthesis and as a potential intermediate in the production of pharmaceuticals and agrochemicals. The compound's reactivity is influenced by the electron-donating nature of the methyl groups and the electron-withdrawing nature of the hydroxyl group, making it a versatile building block in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 121144-97-6

2,4-Dimethylthiophene-3-ol