4433-08-3

Basic information

• Product Name: DEHYDRODIEUGENOL
• Synonyms: DEHYDRODIEUGENOL;3,3'-Dimethoxy-5,5'-di-2-propenyl[1,1'-biphenyl]-2,2'-diol;3,3'-Dimethoxy-5,5'-diallyl-1,1'-biphenyl-2,2'-diol;3,3'-Dimethoxy-5,5'-diallylbiphenyl-2,2'-diol;Bis-EUG
• CAS NO: 4433-08-3
• Molecular Formula: C₂₀H₂₂O₄
• Molecular Weight: 326.39
• Mol File: 4433-08-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DEHYDRODIEUGENOL(CAS DataBase Reference)
• NIST Chemistry Reference: DEHYDRODIEUGENOL(4433-08-3)
• EPA Substance Registry System: DEHYDRODIEUGENOL(4433-08-3)

Safety Data

• Hazardous Substances Data: 4433-08-3(Hazardous Substances Data)

Usage

Description

DEHYDRODIEUGENOL, a derivative of magnolol and a dimer of eugenol, is a compound with significant biological activities. It possesses the ability to inhibit α-Glucosidase, an enzyme involved in the breakdown of carbohydrates, making it a promising candidate for various applications in the pharmaceutical and healthcare industries.

Uses

Used in Pharmaceutical Industry:
DEHYDRODIEUGENOL is used as an α-Glucosidase Inhibitor for its ability to regulate carbohydrate metabolism and potentially manage blood sugar levels. This application can be particularly beneficial for individuals with diabetes or those at risk of developing the condition.
Used in Healthcare Industry:
In the healthcare industry, DEHYDRODIEUGENOL is utilized for its potential role in managing and treating diabetes. By inhibiting α-Glucosidase, it can help control the rate at which carbohydrates are broken down and absorbed into the bloodstream, thus contributing to better blood sugar management.

Upstream product

• 67-56-1 methanol 
• 97-53-0 4-allylguaiacol 

Downstream Products

• 676270-23-8 Carbonic acid 5,5'-diallyl-2'-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyloxycarbonyloxy)-3,3'-dimethoxy-biphenyl-2-yl ester (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 

Relevant articles and documents

Electrochemical Methoxylation of Allyl and Propenyl Derivatives of Phenol and Phenol Ethers

Anodic oxidation of a methanolic solution of a number of phenols and phenol ethers (anethole, estragole, safrole, isosafrole, eugenol, and isoeugenol) in a single cell at constant current, with use of sodium methoxide or sodium methoxide-sodium perchlorate as the supporting electrolyte, afforded substitution and addition products, some of them not described previously in the literature.