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3,4-dihydro-3-(4-methoxyphenyl)-2H-1-benzopyran-6,7-diol, also known as 3,4-dihydroxy-6,7-dimethoxy-2-phenylchroman, is a flavonoid derivative with potential antioxidant, anti-inflammatory, and neuroprotective properties. It is a chemical compound found in certain plants and has been studied for its potential therapeutic effects. Research suggests that 3,4-dihydro-3-(4-methoxyphenyl)-2H-1-benzopyran-6,7-diol may have protective effects against oxidative stress and inflammation, making it a promising candidate for the development of new drugs for the treatment of various conditions. Its chemical structure and properties make it an interesting target for further investigation in pharmacological and medicinal research.

76397-87-0

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76397-87-0 Usage

Uses

Used in Pharmaceutical Industry:
3,4-dihydro-3-(4-methoxyphenyl)-2H-1-benzopyran-6,7-diol is used as a potential therapeutic agent for its antioxidant, anti-inflammatory, and neuroprotective properties. Its protective effects against oxidative stress and inflammation make it a candidate for the development of new drugs for the treatment of various conditions.
Used in Nutraceutical Industry:
3,4-dihydro-3-(4-methoxyphenyl)-2H-1-benzopyran-6,7-diol is used as a dietary supplement or functional food ingredient for its potential health benefits, including antioxidant and anti-inflammatory properties. Its presence in certain plants may contribute to the overall health-promoting effects of these natural sources.
Used in Cosmetic Industry:
3,4-dihydro-3-(4-methoxyphenyl)-2H-1-benzopyran-6,7-diol is used as an active ingredient in cosmetic products for its potential skin health benefits, such as antioxidant and anti-inflammatory effects. Its presence in skincare formulations may help protect the skin from oxidative stress and inflammation, promoting a healthier and more youthful appearance.
Used in Research and Development:
3,4-dihydro-3-(4-methoxyphenyl)-2H-1-benzopyran-6,7-diol is used as a subject of scientific research and development for its potential applications in various fields, including pharmacology, medicine, and nutraceuticals. Its unique chemical structure and properties make it an interesting target for further investigation and exploration of its therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 76397-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,9 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76397-87:
(7*7)+(6*6)+(5*3)+(4*9)+(3*7)+(2*8)+(1*7)=180
180 % 10 = 0
So 76397-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O4/c1-19-13-4-2-10(3-5-13)12-6-11-7-14(17)15(18)8-16(11)20-9-12/h2-5,7-8,12,17-18H,6,9H2,1H3

76397-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenyl)-3,4-dihydro-2H-chromene-6,7-diol

1.2 Other means of identification

Product number -
Other names 6,7-Dihydroxy-4-methoxyisoflavan

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:76397-87-0 SDS

76397-87-0Relevant academic research and scientific papers

Structure-activity relationship studies of flavonoids as potent inhibitors of human platelet 12-hLO, reticulocyte 15-hLO-1, and prostate epithelial 15-hLO-2

Vasquez-Martinez, Yesseny,Ohri, Rachana V.,Kenyon, Victor,Holman, Theodore R.,Sepulveda-Boza, Silvia

, p. 7408 - 7425 (2008/09/18)

Human lipoxygenase (hLO) isozymes have been implicated in a number of disease states and have attracted much attention with respect to their inhibition. One class of inhibitors, the flavonoids, have been shown to be potent lipoxygenase inhibitors but their study has been restricted to those compounds found in nature, which have limited structural variability. We have therefore carried out a comprehensive study to determine the structural requirements for flavonoid potency and selectivity against platelet 12-hLO, reticulocyte 15-hLO-1, and prostate epithelial 15-hLO-2. We conclude from this study that catechols are essential for high potency, that isoflavones and isoflavanones tend to select against 12-hLO, that isoflavans tend to select against 15-hLO-1, but few flavonoids target 15-hLO-2.

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