7-Methoxybenzo[b]thiophene is an organic compound characterized by its fused ring structure, which includes a benzene ring and a thiophene ring. The presence of a methoxy group (-OCH3) at the 7-position of the benzo[b]thiophene framework enhances its solubility and reactivity. This compound typically exhibits properties such as being a pale yellow to brown solid, with a relatively low melting point. It is known for its potential applications in organic electronics, particularly in organic light-emitting diodes (OLEDs) and organic photovoltaics, due to its ability to facilitate charge transport. Additionally, 7-Methoxybenzo[b]thiophene may exhibit interesting photophysical properties, making it a subject of study in materials science and organic chemistry. Its synthesis often involves methods such as electrophilic substitution or coupling reactions. As with many organic compounds, it is essential to handle it with care, considering its potential toxicity and environmental impact.

7-Methoxybenzo[b]thiophene

88791-08-6: 7-Methoxybenzo[b]thiophene, 7-Methoxybenzothiophene, Benzo[b]thien-7-yl methyl ether, Benzo[b]thiophen-7-yl methyl ether, Benzo[b]thiophen-7-ylmethyl ether, Benzo[b]thiophene, 7-methoxy-

7-Methoxybenzo[b]thiophene is a chiral sulfonamide that has been shown to inhibit the activity of acetyl-coa carboxylase, which is an enzyme involved in fatty acid oxidation. It also inhibits the activity of dehydrative sulfonanilides and sulfoxides. This drug has been shown to be effective in rats orally, with a half-life of approximately 3 hours. The oral bioavailability is enhanced by aromatization and sulfonanilide metabolism. 7-Methoxybenzo[b]thiophene exhibits moderate metabolic stability and is metabolized through acetylation, deacetylation, or hydroxylation reactions.

CAS 88791-08-6: 7-Methoxybenzo[b]thiophene

7-Methoxybenzo[b]thiophene

Ref: 3D-NDA79108

7-Methoxybenzo[b]thiophene

Ref: IN-DA008B3V

7-Methoxybenzo[b]thiophene

Ref: 10-F781098

7-Methoxybenzo[b]thiophene

Ref: 54-OR84325