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1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone is a chemical compound characterized by its unique molecular structure that features a benzofuran ring system with a hydroxy group, two methoxy groups, and a carbonyl group attached. 1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone is known for its potential pharmacological properties and versatile chemical structure, which makes it a promising candidate for organic synthesis and drug discovery research.

6938-22-3

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6938-22-3 Usage

Uses

Used in Pharmaceutical Development:
1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone is used as a target compound for pharmaceutical development due to its potential antioxidant, anti-inflammatory, and anticancer activities. Its unique structure allows for modification and derivatization, enabling the creation of new drugs with improved therapeutic effects.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone serves as a valuable intermediate or building block for the synthesis of more complex molecules with diverse applications.
Used in Drug Discovery Research:
1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone is utilized as a subject of drug discovery research, where its pharmacological properties are explored and harnessed for the development of novel therapeutic agents.
Used in Antioxidant Applications:
As a compound with potential antioxidant properties, 1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone is used in the development of antioxidants that can protect cells from oxidative stress and related diseases.
Used in Anti-inflammatory Applications:
1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone is also used in the development of anti-inflammatory agents, targeting the reduction of inflammation and associated conditions.
Used in Anticancer Applications:
1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone is explored for its potential as an anticancer agent, with the aim of developing new treatments for various types of cancer.
Used in Chemical Modification and Derivatization:
The versatile chemical structure of 1-(6-hydroxy-4,7-dimethoxy-2,3-dihydro-1-benzofuran-5-yl)ethanone allows for its use in chemical modification and derivatization processes, leading to the creation of new drugs with enhanced therapeutic effects and improved pharmacokinetic profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 6938-22-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6938-22:
(6*6)+(5*9)+(4*3)+(3*8)+(2*2)+(1*2)=123
123 % 10 = 3
So 6938-22-3 is a valid CAS Registry Number.

6938-22-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydrokhellinone

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-4,7-dimethoxy-5-acetyl-cumaran

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6938-22-3 SDS

6938-22-3Relevant academic research and scientific papers

Synthesis and biological evaluation of chalcones as inhibitors of the voltage-gated potassium channel Kv1.3

Cianci, Julia,Baell, Jonathan B.,Flynn, Bernard L.,Gable, Robert, W.,Mould, Jorgen A.,Paul, Dharam,Harvey, Andrew J.

, p. 2055 - 2061 (2008/12/20)

Chalcone derivatives of the natural product khellinone were synthesised and screened for bioactivity against the voltage-gated potassium channel Kv1.3. X-ray crystallography was employed to investigate relationships between the structure and function of a

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