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2-(3-Hydroxy-2,4-dimethoxyphenyl)benzofuran-6-ol is a complex organic compound with the molecular formula C17H14O6. It is characterized by a benzofuran ring, which is a fusion of a benzene ring and a furan ring, and a hydroxyl group attached to the 3-position of a phenyl group. This phenyl group is further substituted with two methoxy groups at the 2 and 4 positions. The compound is known for its potential biological activities and is often studied in the context of natural products and pharmaceutical research. It is typically synthesized through multi-step organic reactions and can be found in certain plants, where it may contribute to their medicinal properties. The compound's structure and properties make it a subject of interest for chemists and biologists alike, as it may have applications in the development of new drugs and therapeutic agents.

3784-75-6

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3784-75-6 Usage

Molecular structure

2-(3-Hydroxy-2,4-dimethoxyphenyl)benzofuran-6-ol has a complex molecular structure with a benzofuran ring, a hydroxy group, and two methoxy groups.

Class of compounds

It belongs to the benzofuran class of compounds, which are organic compounds consisting of a furan ring fused with a benzene ring.

Solubility

The hydroxy group present in the compound gives it some solubility in water, making it more soluble than other compounds lacking this group.

Lipophilicity

The presence of two methoxy groups in the compound makes it more lipophilic, meaning it can dissolve in lipids and fats, which can be beneficial for its absorption and distribution in the body.

Anti-inflammatory properties

The compound also has potential anti-inflammatory properties, which can help reduce inflammation in the body and may be useful in treating various inflammatory conditions.

Anti-cancer properties

2-(3-Hydroxy-2,4-dimethoxyphenyl)benzofuran-6-ol has shown potential anti-cancer properties, making it a subject of interest for pharmaceutical research. This could lead to the development of new cancer treatments or therapies.

Pharmaceutical research

Due to its antioxidant, anti-inflammatory, and anti-cancer properties, the compound is of interest for pharmaceutical research, which may lead to the development of new drugs or therapies for various diseases.

Skincare and cosmetic applications

The compound's properties, such as its antioxidant and anti-inflammatory effects, may also make it useful in the development of skincare and cosmetic products, potentially benefiting skin health and appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 3784-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3784-75:
(6*3)+(5*7)+(4*8)+(3*4)+(2*7)+(1*5)=116
116 % 10 = 6
So 3784-75-6 is a valid CAS Registry Number.

3784-75-6Downstream Products

3784-75-6Relevant academic research and scientific papers

A short-step convenient synthesis of 2-phenylbenzofuran from 3-phenylcoumarin

Kinoshita, Takeshi,Ichinose, Koji

, p. 1641 - 1654 (2007/10/03)

The reaction mechanism of chemical conversion of (E)-β-[2-hydroxylphenylethylene]benzeneethanol into 2-phenylbenzofuran by DDQ, which involves loss of one carbon unit, was characterized and described. Five naturally occurring 2-phenylbenzofurans of not only the isoflavonoid but also stilbenoid origin were synthesized by use of this chemical scheme, which proved that this new scheme is a useful tool for quick synthesis of 2-phenylbenzofurans.

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