CAS 63675-74-1

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

Description:

6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophene, with the CAS number 63675-74-1, is an organic compound characterized by its unique structure that includes a thiophene ring fused to a benzene derivative. This compound features methoxy groups, which are electron-donating substituents that can influence its chemical reactivity and solubility. The presence of the thiophene moiety suggests potential applications in organic electronics, such as in organic light-emitting diodes (OLEDs) or organic photovoltaics, due to its ability to facilitate charge transport. Additionally, the methoxy groups may enhance its solubility in organic solvents, making it suitable for various synthetic applications. The compound's aromatic nature and functional groups may also contribute to its potential biological activity, warranting further investigation in medicinal chemistry. Overall, 6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiophene represents a versatile structure with implications in both materials science and pharmacology.

Formula: C₁₆H₁₄O₂S

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: O(C)C1=CC=C(C=2SC=3C(C2)=CC=C(OC)C3)C=C1

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

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

CAS: 63675-74-1

Purity: 95.0%

Color and Shape: Solid, Powder

Molecular weight: 270.3500061035156

Ref: 10-F238785

6-Methoxy-2-(4-methoxyphenyl)benzobithiophene

CAS: 63675-74-1

Formula: C₁₆H₁₄O₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 270.3462

Ref: IN-DA0039GR

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

CAS: 63675-74-1

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

Purity: 98%

Molecular weight: 270.35g/mol

Ref: 54-OR75675

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

Controlled Product

CAS: 63675-74-1

Formula: C₁₆H₁₄O₂S

Color and Shape: Neat

Molecular weight: 270.35

Ref: 86-MM0738.07

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

CAS: 63675-74-1

Formula: C₁₆H₁₄O₂S

Molecular weight: 270.35

Ref: ST-EA-CP-R2010

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

Controlled Product

CAS: 63675-74-1

Applications Intermediate in the production of Raloxifene impurities.
References Schopfer, U., et al.: J. Med. Chem., 45, 1399 (2002), Liu, J., et al.: Chem. Res. Toxicol., 18, 1485 (2005), Yang, C., et al.: Bioorg. Med. Chem. Lett., 15, 1505 (2005),

Formula: C₁₆H₁₄O₂S

Color and Shape: Neat

Molecular weight: 270.35

Ref: TR-M263060

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

CAS: 63675-74-1

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.

Formula: C₁₆H₁₄O₂S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 270.35 g/mol

Ref: 3D-FM25206