CAS 3781-90-6

Benzo[b]thiophene, 4-methoxy-

Description:

Benzo[b]thiophene, 4-methoxy- is an organic compound characterized by a fused ring structure that includes a benzene ring and a thiophene ring, with a methoxy group (-OCH3) attached to the fourth position of the benzo[b]thiophene framework. This compound typically exhibits properties associated with aromatic compounds, such as stability and a tendency to undergo electrophilic substitution reactions. The presence of the methoxy group can influence its reactivity and solubility, often enhancing its lipophilicity and potentially affecting its biological activity. Benzo[b]thiophene derivatives are of interest in various fields, including organic synthesis and materials science, due to their unique electronic properties and potential applications in pharmaceuticals and agrochemicals. The compound is generally considered to have low to moderate toxicity, but specific safety data should be consulted for handling and usage. As with many organic compounds, it is important to consider its environmental impact and regulatory status in various jurisdictions.

Formula: C₉H₈OS

Synonyms:

• 4-METHOXY-1-BENZOTHIOPHENE
• Benzo[b]thiophene,4-Methoxy-

Benzo[b]thiophene,4-Methoxy-

CAS: 3781-90-6

Formula: C₉H₈OS

Purity: 95%

Color and Shape: Liquid

Molecular weight: 164.2242

Ref: IN-DA00CACL

4-Methoxybenzo[b]thiophene

CAS: 3781-90-6

4-Methoxybenzo[b]thiophene

Purity: 95%

Molecular weight: 164.229g/mol

Ref: 54-OR73084

4-METHOXYBENZO[B]THIOPHENE

CAS: 3781-90-6

Formula: C₉H₈OS

Purity: 95%

Molecular weight: 164.22

Ref: 10-F501636

4-Methoxybenzo[b]thiophene

CAS: 3781-90-6

4-Methoxybenzo[b]thiophene is a molecule that is activated by fluorescence and emits light as it transfers from an excited state to a lower energy state. This process is called fluorescence, and the emitted light can be detected with ultraviolet (UV) spectroscopy. 4-Methoxybenzo[b]thiophene has been shown to have an olefinic nature, which means it reacts readily with electron-donating groups such as alcohols or phenols. The reaction rate for this compound increases with increasing temperatures and the population of acceptor molecules. It has been studied using photophysical techniques and lipid profile analysis, which measures the lipid content of cells in order to determine their health status.

Formula: C₉H₈OS

Purity: Min. 95%

Molecular weight: 164.22 g/mol

Ref: 3D-DAA78190