4,5-Dihydro-2-methylthiophene is a heterocyclic organic compound characterized by its five-membered ring structure containing both carbon and sulfur atoms. It features a thiophene ring that is partially saturated, which contributes to its unique chemical properties. The presence of a methyl group at the 2-position of the ring enhances its reactivity and influences its physical properties, such as boiling and melting points. This compound is typically a colorless to pale yellow liquid with a distinctive odor, often associated with sulfur-containing compounds. It is soluble in organic solvents and has limited solubility in water. 4,5-Dihydro-2-methylthiophene is of interest in various fields, including organic synthesis and materials science, due to its potential applications in the production of pharmaceuticals, agrochemicals, and as a building block for more complex molecules. Its reactivity can be attributed to the presence of the double bond in the thiophene ring, making it a candidate for various chemical transformations. Safety data should be consulted for handling and storage, as with all chemical substances.

4,5-Dihydro-2-methylthiophene

4610-02-0: 4,5-Dihydro-2-methylthiophene is a heterocyclic organic compound characterized by its five-membered ring structure containing both carbon and sulfur atoms. It features a thiophene ring that is partially saturated, which contributes to its unique chemical properties. The presence of a methyl group at the 2-position of the ring enhances its reactivity and influences its physical properties, such as boiling and melting points. This compound is typically a colorless to pale yellow liquid with a distinctive odor, often associated with sulfur-containing compounds. It is soluble in organic solvents and has limited solubility in water. 4,5-Dihydro-2-methylthiophene is of interest in various fields, including organic synthesis and materials science, due to its potential applications in the production of pharmaceuticals, agrochemicals, and as a building block for more complex molecules. Its reactivity can be attributed to the presence of the double bond in the thiophene ring, making it a candidate for various chemical transformations. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 4610-02-0

4,5-Dihydro-2-methylthiophene

Thiophene Impurity 1

Ref: 4Z-T-194006