6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophene

CAS: 63675-74-1

Ref. 3D-FM25206

Product Information

• Name: 6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophene
• Synonyms: 2-(4-Methoxyphenyl)-6-methoxybenzo[b]thiophene, 2-(4-Methoxyphenyl)-6-methoxybenzothiophene, 4-(2-Piperidnoethoxy)Benzoic Acid Hydrochloride, 4-(6-Methoxy-1-Benzothiophen-2-Yl)Phenyl Methyl Ether, 6-Methoxy-2-(4-Methoxyhenyl)Benzo[B]Thiophene, 6-Methoxy-2-(4-Methoxyphenyl) Thianaphthene, 6-Methoxy-2-(4-Methoxyphenyl)-1-Benzothiophene, 6-Methoxy-2-(4-Methoxyphenyl)Benzo[B]Thiophene, 6-Methoxy-2-(4-Methoxyphenyl)Benzobithiophene, 6-Methoxy-2-(4-methoxyphenyl)benzo [B]thiophen, 6-Methoxy-2-(4-methoxyphenyl)benzothiophene, Benzo[b]thiophene, 6-methoxy-2-(4-methoxyphenyl)-
• CAS: 63675-74-1

Description

6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophene (6MBT) is a mesomorphic, acid catalyst that has been used to synthesize polyphosphoric acid. It reacts with chloride to form 6-chloro-2-(4-methoxyphenyl)benzo[b]thiophene, which can be converted to the desired product by sulfoxide. The reaction time for this process is relatively short and the yield is high. 6MBT can also be used as a semiconductor in devices such as solar cells and electronic displays. The photoelectric effect of 6MBT was demonstrated in 1972, when it was found that electron emission from a photocurrent could be obtained at room temperature. This property has been shown to be due to the molecule's absorption of light energy and subsequent conversion into electrical energy.

• Brand: Biosynth

Chemical properties

• Molecular weight: 270.35 g/mol
• Formula: C₁₆H₁₄O₂S
• Purity: Min. 95%
• Color/Form: Powder
• InChI: InChI=1S/C16H14O2S/c1-17-13-6-3-11(4-7-13)15-9-12-5-8-14(18-2)10-16(12)19-15/h3-10H,1-2H3
• InChI key: InChIKey=HRWAGCVMOGWQJF-UHFFFAOYSA-N
• SMILES: COc1ccc(-c2cc3ccc(OC)cc3s2)cc1