(2R)-2,3-Dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one - Names and Identifiers
Name | (2R)-2,3-Dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
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Synonyms | Neophellamuretin (2R,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one (2R)-2,3-Dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one (2R)-2,3-DIHYDRO-3Β,5,7-TRIHYDROXY-2Α-(4-HYDROXYPHENYL)-8-(3-METHYL-2-BUTENYL)-4H-1-BENZOPYRAN-4-ONE 4H-1-Benzopyran-4-one, 2,3-dihydro-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-, (2R,3R)-
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CAS | 52589-20-5
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(2R)-2,3-Dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one - Physico-chemical Properties
Molecular Formula | C20H20O6
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Molar Mass | 356.37 |
Storage Condition | 2-8℃ |
(2R)-2,3-Dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one - Introduction
(2R)-2,3-dihydroxy-3β, 5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one is a compound also known as (2R)-naringenin chelcone. Here are some details about this compound:
Nature:
-Appearance:(2R)-2,3-dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one is a white or light yellow crystalline powder.
-Solubility: Its solubility in water is low, but it can be dissolved in organic solvents.
Use:
-Cosmetics industry:(2R)-2,3-dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one has antioxidant and anti-inflammatory activity, it is often used in cosmetics, skin care products, creams and anti-aging products.
-Pharmaceutical Research: The compound has potential pharmacological activity and is being investigated for its possible use in the treatment of cancer, cardiovascular disease and inflammation.
Method:
(2R)-2,3-dihydro-3β,5,7-trihydroxy-2α-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one is usually prepared by synthetic methods. The specific method can be:
1. Starting from citric acid ester, add appropriate reagents in a series of chemical reactions to make it undergo reaction steps such as oxidation, condensation and dehydration, and finally obtain the target compound.
Safety Information:
Last Update:2024-04-09 02:00:53